Garden bean named HMX0164494

ABSTRACT

Novel garden bean cultivars, such as bean designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 are disclosed. In some embodiments, the invention relates to the seeds of garden bean HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, to the plants and plant parts of garden bean HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, and to methods for producing a garden bean plant by crossing the garden bean HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 with itself or another garden bean plant. The invention further relates to methods for producing other garden bean plants derived from the garden bean HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a divisional application of U.S. patent application Ser. No. 15/215,230, filed on Jul. 20, 2016, which is herein incorporated by reference in its entirety for all purposes.

FIELD OF THE INVENTION

The present invention relates to the field of agriculture, to new and distinctive garden bean cultivar (Phaseolus vulgaris), such as cultivars designated HMX4104, HMX0164423, HMX0164444, HMX0164476, and HMX0164494, and to methods of making and using such plants.

BACKGROUND OF THE INVENTION

The following description includes information that may be useful in understanding the present invention. It is not an admission that any of the information provided herein is prior art or relevant to the presently claimed inventions, or that any publication specifically or implicitly referenced is prior art.

Garden bean, Phaseolus vulgaris L., is an important and valuable vegetable crop. Thus, a continuing goal of garden bean plant breeders is to develop stable, high yielding garden bean cultivar that are agronomically sound or unique. The reasons for this goal are to maximize the amount of yield produced on the land. To accomplish this goal, the garden bean breeder must select and develop garden bean plants that have traits that result in superior cultivars.

SUMMARY OF THE INVENTION

The following embodiments and aspects thereof are described in conjunction with systems, tools and methods which are meant to be exemplary, not limiting in scope.

In various embodiments, one or more of the above-described problems have been reduced or eliminated, while other embodiments are directed to other improvements.

According to the invention, in some embodiments, there are provided novel garden bean cultivar, designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. This invention thus relates to the seeds of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, to the plants or parts thereof of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, to plants or parts thereof consisting essentially of the phenotypic and morphological characteristics of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, and/or having all the physiological and morphological characteristics of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 and/or having one or more or all of the characteristics of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 listed in Tables 1 to 5 including, but not limited to, as determined at the 5% significance level when grown in the same environmental condition, and/or having the physiological and morphological characteristics of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 listed in Tables 1 to 5 including but not limited to as determined at the 5% significance level when grown in the same environmental condition, and/or having all the physiological and morphological characteristics of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 listed in Tables 1 to 5 including but not limited to as determined at the 5% significance level when grown in the same environmental condition and/or having all the physiological and morphological characteristics of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 listed in Tables 1 to 5 when grown in the same environmental condition. The invention also relates to variants, mutants and trivial modifications of the seed or plant of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494.

Plant parts of the garden bean cultivar of the present invention are also provided, such as a pod, leaf, flower, cell, pollen or ovule obtained from the plant cultivar. The present invention provides pods of the garden bean cultivar of the present invention. Such pods could be used as fresh products for consumption or in processes resulting in processed products such as food products comprising one or more harvested part of the garden bean plant HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, for example harvested pods. The harvested part or food product can be or can comprise the garden bean pods of the garden bean plant HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. The food products might have undergone one or more processing steps such as, but not limited to cutting, washing, mixing, frizzing, canning, etc. All such products are part of the present invention.

The plants and seeds of the present invention include those that may be of an essentially derived variety as defined in section 41(3) of the Plant Variety Protection Act of the United States of America, i.e., a variety that is predominantly derived from garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 or from a variety that i) is predominantly derived from garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, while retaining the expression of the essential characteristics that result from the genotype or combination of genotypes of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494; ii) is clearly distinguishable from garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494; and iii) except for differences that result from the act of derivation, conforms to the initial variety in the expression of the essential characteristics that result from the genotype or combination of genotypes of the initial variety or cultivar.

In another aspect, the present invention provides regenerable cells. In some embodiments, the regenerable cells are for use in tissue culture of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. In some embodiments, the tissue culture is capable of regenerating plants consisting essentially of the phenotypic and morphological characteristics of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, and/or having all the phenotypic and morphological characteristics of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, and/or having the physiological and morphological characteristics of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, and/or having the characteristics of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. In one embodiment, the regenerated plants have the characteristics of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 listed in Tables 1 to 5 including but not limited to as determined at the 5% significance level when grown in the same environmental condition. In some embodiments, the plant parts and cells used to produce such tissue cultures can be embryos, meristematic cells, seeds, callus, pollen, leaves, anthers, pistils, roots, root tips, stems, petioles, pods, cotyledons, hypocotyls, ovaries, seed coat, endosperm, flowers, axillary buds or the like. Protoplasts produced from such tissue culture are also included in the present invention. The garden bean shoots, roots and whole plants regenerated from the tissue culture, as well as the pods produced by said regenerated plants are also part of the invention. In some embodiments, the whole plants regenerated from the tissue culture have one, more than one, or all of the physiological and morphological characteristics of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 listed in Tables 1 to 5 including but not limited to when grown in the same environmental condition.

The invention also discloses methods for vegetatively propagating a plant of the present invention. In some embodiments, the methods comprise collecting a part of a garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 and regenerating a plant from said part. In some embodiments, the part can be for example a leaf cutting that is rooted into an appropriate medium according to techniques known by the one skilled in the art. Plants, plant parts and pods thereof produced by such methods are also included in the present invention. In another aspect, the plants and pods thereof produced by such methods consist essentially of the phenotypic and morphological characteristics of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, and/or having all the phenotypic and morphological characteristics of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, and/or having the physiological and morphological characteristics of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, and/or having the characteristics of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. In some embodiments, plant produced by such method consist of one, more than one, or all phenotypic and morphological characteristics of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 listed in Tables 1 to 5 including but not limited to when grown in the same environmental condition.

Further included in the invention are methods for producing pods from the garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. In some embodiments, the methods comprise growing a garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 to produce a garden bean pod. In some embodiments, the methods further comprise harvesting the garden bean pod. Such garden bean pods thereof are part of the present invention.

Also included in this invention are methods for producing a garden bean plant. In some embodiments, the garden bean plant is produced by crossing the garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 with itself or another garden bean plant. In some embodiment, the other plant can be a garden bean hybrid or line. When crossed with itself, i.e. when HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 is crossed with another garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 or self-pollinated, garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 will be conserved (e.g. as an inbred). When crossed with another, different garden bean plant, an F1 hybrid seed is produced if the different garden bean plant is an inbred and a “three-way cross” seed is produced if the different garden bean plant is a hybrid. Such F1 hybrid seed and three-way hybrid seeds and plants produced by growing said F1 and three-way hybrid seeds are included in the present invention. Methods for producing a F1 and three-way hybrid garden bean seed comprising crossing garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 garden bean plant with a different garden bean line or hybrid and harvesting the resultant hybrid garden bean seed are also part of the invention. The hybrid garden bean seeds produced by the methods comprising crossing garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 garden bean plant with a different garden bean plant and harvesting the resultant hybrid garden bean seed are included in the invention, as are included the hybrid garden bean plants or parts thereof and seeds produced by said grown hybrid garden bean plants.

Further included in the invention are methods for producing a garden bean seed and plants made thereof. In some embodiments, the methods comprise self-pollinating the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 and harvesting the resultant seeds. Garden bean seeds produced by such method are also part of the invention.

In another embodiment, this invention relates to methods for producing other garden bean plants derived from garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 and to the garden bean plants derived by the use of those methods.

In some embodiments, such methods for producing a garden bean plant derived from the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 comprise (a) self-pollinating the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 plant at least once to produce a progeny plant derived from garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494; In some embodiments, the methods further comprise (b) crossing the progeny plant derived from garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 with itself or a second garden bean plant to produce a seed of a progeny plant of a subsequent generation; In some embodiments, the methods further comprise (c) growing the progeny plant of the subsequent generation; In some embodiment, the method further comprises (d) crossing the progeny plant of the subsequent generation with itself or a second garden bean plant to produce a garden bean plant further derived from the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. In further embodiments, steps (b), (c) and/or (d) are repeated for at least 1, 2, 3, 4, 5, 6, 7, 8, or more generation to produce a garden bean plant derived from the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. In some embodiments, within each crossing cycle, the second plant is the same plant as the second plant in the last crossing cycle. In some embodiments, within each crossing cycle, the second plant is different from the second plant in the last crossing cycle.

Another method for producing a garden bean plant derived from the variety HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, comprises the steps of: (a) crossing the garden bean plant HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 plant with a second garden bean plant to produce a progeny plant derived from garden bean plant HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494; In some embodiments, the method further comprises (b) crossing the progeny plant derived from garden bean plant HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 with itself or a second garden bean plant to produce a seed of a progeny plant of a subsequent generation; In some embodiments, the method further comprises (c) growing a progeny plant of the subsequent generation; In some embodiments, the method further comprises (d) crossing the progeny plant of the subsequent generation with itself or a second garden bean plant to produce a garden bean plant derived from the garden bean plant HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. In a further embodiment, steps (b), (c) and/or (d) are repeated for at least 1, 2, 3, 4, 5, 6, 7, 8, or more generation to produce a garden bean plant derived from the garden bean plant HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. In some embodiments, within each crossing cycle, the second plant is the same plant as the second plant in the last crossing cycle. In some embodiments, within each crossing cycle, the second plant is different from the second plant in the last crossing cycle.

In another aspect, the present invention provides methods of introducing or modifying one or more desired trait(s) into the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 and plants or seeds obtained from such methods. The desired trait(s) may be, but not exclusively, a single gene. In some embodiments, the gene is a dominant allele. In some embodiments, the gene is a partially dominant allele. In some embodiments, the gene is a recessive allele. In some embodiments, the gene or genes will confer such traits as male sterility, herbicide resistance, insect resistance, resistance for bacterial, fungal, mycoplasma or viral disease, increased leaf number, improved shelf life, delayed senescence and tolerance to water stress or heat stress. For the present invention and the skilled artisan, disease is understood to include, but not limited to fungal diseases, viral diseases, bacterial diseases, mycoplasma diseases, or other plant pathogenic diseases and a disease resistant plant will encompass a plant resistant to fungal, viral, bacterial, mycoplasma, and other plant pathogens. The gene or genes may be naturally occurring garden bean gene(s), mutant(s) or genes modified through New Breeding Techniques. In some embodiments, the method for introducing the desired trait(s) is a backcrossing process making use of a series of backcrosses to garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 during which the desired trait(s) is maintained by selection. The single gene conversion plants that can be obtained by the method are included in the present invention.

When dealing with a gene that has been modified, for example through New Breeding Techniques, the trait (genetic modification) could be directly modified into the newly developed line/cultivar such as garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. Alternatively, if the trait is not modified into each newly developed line/cultivar such as garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, another typical method used by breeders of ordinary skill in the art to incorporate the modified gene is to take a line already carrying the gene and to use such line as a donor line to transfer the gene into the newly developed line. The same would apply for a naturally occurring trait or one arising from spontaneous or induced mutations.

In some embodiments, the backcross breeding process of garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 comprises (a) crossing garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 with plants that comprise the desired trait(s) to produce F1 progeny plants. In some embodiments, the process further comprises (b) selecting the F1 progeny plants that have the desired trait(s); In some embodiments, the process further comprises (c) crossing the selected F1 progeny plants with the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 plants to produce backcross progeny plants; In some embodiments, the process further comprises (d) selecting for backcross progeny plants that have the desired trait(s) and physiological and morphological characteristics of the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 to produce selected backcross progeny plants; In some embodiments, the process further comprises (e) repeating steps (c) and (d) one, two, three, four, five six, seven, eight, nine or more times in succession to produce selected, second, third, fourth, fifth, sixth, seventh, eighth, ninth or higher backcross progeny plants that have the desired trait(s) and consist essentially of the phenotypic and morphological characteristics of the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, and/or have all the phenotypic and morphological characteristics of the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, and/or have the desired trait(s) and the physiological and morphological characteristics of the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 as determined in Tables 1 to 5, including but not limited to at a 5% significance level when grown in the same environmental conditions. The garden bean plants or seeds produced by the method are also part of the invention, as are the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 that comprise the desired trait(s). Backcrossing breeding methods, well known to one skilled in the art of plant breeding will be further developed in subsequent part of the specification.

In an embodiment of this invention is a method of making a backcross conversion of garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. In some embodiments, the method comprises crossing garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 with a donor plant comprising a mutant gene(s), a naturally occurring gene(s), or a gene(s) and/or sequences modified through the use of New Breeding Techniques, conferring one or more desired trait to produce F1 progeny plant. In some embodiment, the method further comprises selecting an F1 progeny plant comprising the naturally occurring gene(s), mutant gene(s) or modified gene(s) and/or sequence conferring the one or more desired trait. In some embodiments, the method further comprises backcrossing the selected progeny plant to the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. This method may further comprise the step of obtaining a molecular marker profile of the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 and using the molecular marker profile to select for a progeny plant with the desired trait and the molecular marker profile of the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. The plants or parts thereof produced by such methods are also part of the present invention.

In some embodiments of the invention, the number of loci that may be backcrossed into the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 is at least 1, 2, 3, 4, 5 or more. A single locus may contain one or several genes. A single locus conversion also allows for making one or more site specific changes to the plant genome, such as, without limitation, one or more nucleotide change, deletion, insertions, etc. In some embodiments, the single locus conversion is performed by genome editing, a.k.a. genome editing with engineered nucleases (GEEN). In some embodiments, the genome editing comprises using one or more engineered nucleases. In some embodiments, the engineered nucleases include, but are not limited to Zinc finger nucleases (ZFNs), Transcription Activator-Like Effector Nucleases (TALENs), the CRISPR/Cas system, engineered meganuclease, re-engineered homing endonucleases, and endonucleases for DNA guided genome editing (Gao et al., Nature Biotechnology (2016), doi: 10.1038/nbt.3547). In some embodiments, the single locus conversion changes one or several nucleotides of the plant genome. Such genome editing techniques are some of the techniques now known by a person skilled in the art and herein are collectively referred to as ‘New Breeding Techniques’. The invention further provides methods for developing garden bean plants in a garden bean plant breeding program using plant breeding techniques including but not limited to, recurrent selection, backcrossing, pedigree breeding, molecular marker (Isozyme Electrophoresis, Restriction Fragment Length Polymorphisms (RFLPs), Randomly Amplified Polymorphic DNAs (RAPDs), Arbitrarily Primed Polymerase Chain Reaction (AP-PCR), DNA Amplification Fingerprinting (DAF), Sequence Characterized Amplified Regions (SCARs), Amplified Fragment Length Polymorphisms (AFLPs), and Simple Sequence Repeats (SSRs) which are also referred to as Microsatellites, Single Nucleotide Polymorphisms (SNPs), etc.) enhanced selection, genetic marker enhanced selection and transformation. Seeds, garden bean plants, and parts thereof produced by such breeding methods are also part of the invention.

The invention also relates to variants, mutants and trivial modifications of the seed or plant of the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. Variants, mutants and trivial modifications of the seed or plant of garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 can be generated by methods available to one skilled in the art, including but not limited to, mutagenesis (e.g., chemical mutagenesis, radiation mutagenesis, transposon mutagenesis, insertional mutagenesis, signature tagged mutagenesis, site-directed mutagenesis, and natural mutagenesis), knock-outs/knock-ins, antisense, RNA interference and other techniques such as the New Breeding Techniques. For more information of mutagenesis in plants, such as agents, protocols, see Acquaah et al. (Principles of plant genetics and breeding, Wiley-Blackwell, 2007, ISBN 1405136464, 9781405136464, which is herein incorporated by reference in its entity).

The invention also relates to a mutagenized population of the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 and methods of using such populations. In some embodiments, the mutagenized population can be used in screening for new garden bean plants which comprises one or more or all of the morphological and physiological characteristics of garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. In some embodiments, the new garden bean plants obtained from the screening process comprise all of the morphological and physiological characteristics of the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, and one or more additional or different morphological and physiological characteristics that garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 does not have.

This invention also is directed to methods for producing a garden bean plant by crossing a first parent garden bean plant with a second parent garden bean plant wherein either the first or second parent garden bean plant is a garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. Further, both first and second parent garden bean plants can come from the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. Further, the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 can be self-pollinated i.e. the pollen of a garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 can pollinate the ovule of the same garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, respectively. When crossed with another garden bean plant, a hybrid seed is produced. Such methods of hybridization and self-pollination are well known to those skilled in the art of breeding.

A garden bean cultivar such as garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 has been produced through several cycles of self-pollination and is therefore to be considered as a homozygous plant or line. An inbred line can also be produced though the dihaploid system which involves doubling the chromosomes from a haploid plant or embryo thus resulting in an inbred line that is genetically stable (homozygous) and can be reproduced without altering the inbred line: Haploid plants could be obtained from haploid embryos that might be produced from microspores, pollen, anther cultures, ovary cultures or spontaneous haploidy. The haploid embryos may then be doubled by chemical treatments such as by colchicine or be doubled autonomously. The haploid embryos may also be grown into haploid plants and treated to induce the chromosome doubling. In either case, fertile homozygous plants are obtained. A hybrid variety is classically created through the fertilization of an ovule from an inbred parental line by the pollen of another, different inbred parental line. Due to the homozygous state of the inbred line, the produced gametes carry a copy of each parental chromosome. As both the ovule and the pollen bring a copy of the arrangement and organization of the genes present in the parental lines, the genome of each parental line is present in the resulting F1 hybrid, theoretically in the arrangement and organization created by the plant breeder in the original parental line.

As long as the homozygosity of the parental lines is maintained, the resulting hybrid cross shall be stable. The F1 hybrid is then a combination of phenotypic characteristics issued from two arrangement and organization of genes, both created by a man skilled in the art through the breeding process.

Still further, this invention also is directed to methods for producing a garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494-derived garden bean plant by crossing garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 with a second garden bean plant. In some embodiments, the method further comprises obtaining a progeny seed from the cross. In some embodiment, the method further comprises growing the progeny seed, and possibly repeating the crossing and growing steps with the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494-derived plant from 0 to 7, or more times. Thus, any such methods using the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 are part of this invention: selfing, backcrosses, hybrid production, crosses to populations, and the like. All plants produced using garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 as a parent are within the scope of this invention, including plants derived from garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. In some embodiment, such plants have one, more than one, or all phenotypic and morphological characteristics of garden bean cultivar designated HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 listed in Tables 1 to 5 including but not limited to when grown in the same environmental condition.

Such plants might exhibit additional and desired characteristics or traits such as high seed yield, high seed germination, seedling vigor, early maturity, high yield, disease tolerance or resistance, and adaptability for soil and climate conditions. Consumer-driven traits, such as a preference for a given pod size, shape, color, texture, taste, are other traits that may be incorporated into new garden bean plants developed by this invention.

A garden bean plant can also be propagated vegetatively. A part of the plant, for example a shoot tissue, is collected, and a new plant is obtained from the part. Such part typically comprises an apical meristem of the plant. The collected part is transferred to a medium allowing development of a plantlet, including for example rooting or development of shoots or grafted onto a garden bean plant or a rootstock prepared to support growth of the shoot tissue. This is achieved using methods well-known in the art. Accordingly, in one embodiment, a method of vegetatively propagating a plant of the present invention comprises collecting a part of a plant according to the present invention, e.g. a shoot tissue, and obtaining a plantlet from said part. In one embodiment, a method of vegetatively propagating a plant of the present invention comprises: a) collecting tissue of a plant of the present invention; b) rooting said proliferated shoots to obtain rooted plantlets. In one embodiment, a method of vegetatively propagating a plant of the present invention comprises: a) collecting tissue of a plant of the present invention; b) cultivating said tissue to obtain proliferated shoots; c) rooting said proliferated shoots to obtain rooted plantlets. In one embodiment, such method further comprises growing a plant from said plantlets. In one embodiment, a pod is harvested from said plant.

In some embodiments, the present invention teaches a seed of garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, wherein a representative sample of seed of garden bean cultivar HMX0164494 is deposited under NCIMB No 43481.

In some embodiments, the present invention teaches a garden bean plant, or a part thereof, produced by growing the deposited HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 seed.

In some embodiments, the present invention teaches garden bean plant parts, wherein the garden bean part is selected from the group consisting of: a leaf, a flower, a pod, an ovule, pollen, and a cell.

In some embodiments, the present invention teaches a garden bean plant, or a part thereof, having all of the characteristics of garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 as listed in Tables 1 to 5 of this application, including but not limited to when grown in the same environmental condition.

In some embodiments, the present invention teaches a garden bean plant, or a part thereof, having all of the physiological and morphological characteristics of garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, wherein a representative sample of seed of garden bean plant HMX0164494 was deposited under NCIMB No 43481.

In some embodiments, the present invention teaches a tissue culture of regenerable cells produced from the plant or plant part grown from the deposited garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 seed, wherein cells of the tissue culture are produced from a plant part selected from the group consisting of protoplasts, embryos, meristematic cells, callus, pollen, ovules, flowers, seeds, leaves, roots, root tips, anthers, stems, petioles, pods, axillary buds, cotyledons and hypocotyls. In some embodiments, the plant part includes protoplasts produced from a plant grown from the deposited garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 seed.

In some embodiments, the present invention teaches a garden bean plant regenerated from the tissue culture from a plant grown from the deposited garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 seed, said plant having the characteristics of garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, wherein a representative sample of seed of garden bean cultivar HMX0164494 is deposited under NCIMB No 43481.

In some embodiments, the present invention teaches a garden bean pod produced from plants grown from the deposited garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 seed.

In some embodiments, methods of producing said garden bean pod comprise a) growing the garden bean plant from deposited garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 seed to produce a garden bean pod, and b) harvesting said garden bean pod. In some embodiments, the present invention also teaches a garden bean pod produced by the method of producing garden bean pod as described above.

In some embodiments, the present invention teaches methods for producing a garden bean seed comprising crossing a first parent garden bean plant with a second parent garden bean plant and harvesting the resultant garden bean seed, wherein said first parent garden bean plant and/or second parent garden bean plant is the garden bean plant produced from the deposited garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 seed or a garden bean plant having all of the characteristics of HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 as listed in Tables 1 to 5, including but not limited to when grown in the same environmental condition.

In some embodiments, the present invention teaches methods for producing a bean seed comprising self-pollinating the garden bean plant grown from the deposited garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 seed and harvesting the resultant garden bean seed.

In some embodiments, the present invention teaches the seed produced by any of the above described methods.

In some embodiments, the present invention teaches methods of vegetatively propagating the garden bean plant grown from the deposited garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 seed, said method comprising a) collecting part of a plant grown from the deposited garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 seed and b) regenerating a plant from said part.

In some embodiments, the method further comprises harvesting a pod from said vegetatively propagated plant.

In some embodiments, the present invention teaches the plant, and pods thereof of plants vegetatively propagated from plant parts of plants grown from the deposited garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 seed.

In some embodiments, the present invention teaches methods of producing a garden bean plant derived from the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. In some embodiments, the methods comprise the steps of: (a) self-pollinating the plant grown from the deposited garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 seed at least once to produce a progeny plant derived from garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494; In some embodiment, the method further comprises (b) crossing the progeny derived from garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 with itself or a second garden bean plant to produce a seed of a progeny plant of a subsequent generation; and; (c) growing the progeny plant of a subsequent generation from the seed, and crossing the progeny plant of the subsequent generation with itself or a second garden bean plant to produce a garden bean plant derived from the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. In some embodiments said method further comprises the step of: (d) repeating steps (b) or (c) for at least 1, 2, 3, 4, 5, 6, 7, or more generation to produce a garden bean plant derived from the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494.

In some embodiments, the present invention teaches methods of producing a garden bean plant derived from the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494, the methods comprising the steps of: (a) crossing the plant grown from the deposited garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 seed with a second garden bean plant to produce a progeny plant derived from garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494; In some embodiment, the method further comprises (b) crossing the progeny plant derived from garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 with itself or a second garden bean plant to produce a seed of a progeny plant of a subsequent generation; and; (c) growing a progeny plant of the subsequent generation from the seed; (d) crossing the progeny plant of the subsequent generation with itself or a second garden bean plant to produce a garden bean plant derived from the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494. In some embodiments said method further comprises the steps of: (e) repeating step (b), (c) and/or (d) for at least 1, 2, 3, 4, 5, 6, 7, or more generation to produce a garden bean plant derived from the garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494.

In some embodiments, the present invention teaches plants grown from the deposited garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 seed wherein said plants comprise at least one single locus conversion. In some embodiments said single locus conversion confers said plant with a trait selected from the group consisting of male sterility, male fertility, herbicide resistance, insect resistance, disease resistance, water stress tolerance, heat tolerance, delayed senescence, improved ripening control, long shelf life, and improved salt tolerance when compared to a suitable check plant. In some embodiments, the check plant is a garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494 not having said single locus conversion. In some embodiments, the at least one single locus conversion is an artificially mutated gene or a gene or nucleotide sequence modified through the use of New Breeding Techniques.

In addition to the exemplary aspects and embodiments described above, further aspects and embodiments will become apparent by study of the following descriptions.

DETAILED DESCRIPTION OF THE INVENTION Definitions

In the description and tables that follow, a number of terms are used. In order to provide a clear and consistent understanding of the specification and claims, including the scope to be given such terms, the following definitions are provided:

Allele. An allele is any of one or more alternative forms of a gene which relate to one trait or characteristic. In a diploid cell or organism, the two alleles of a given gene occupy corresponding loci on a pair of homologous chromosomes.

Backcrossing. Backcrossing is a process in which a breeder repeatedly crosses hybrid progeny back to one of the parents, for example, a first generation hybrid F₁ with one of the parental genotype of the F₁ hybrid.

Bean yield (tons/acre). The yield in tons/acre is the actual yield of the bean pods at harvest.

Determinate plant. A determinate plant will grow to a fixed number of nodes while an indeterminate plant continues to grow during the season.

Emergence. The rate that the seed germinates and sprouts out of the ground.

Essentially all the physiological and morphological characteristics. A plant having essentially all the physiological and morphological characteristics means a plant having the physiological and morphological characteristics, except for the characteristics derived from the converted gene.

Field holding ability. A bean plant that has field holding ability means a plant having pods that remain smooth and retain their color even after the seed is almost fully developed. Immunity to disease(s) and or insect(s). A bean plant which is not subject to attack or infection by specific disease(s) and or insect(s) is considered immune.

Intermediate resistance to disease(s) and or insect(s). A bean plant that restricts the growth and development of specific disease(s) and or insect(s), but may exhibit a greater range of symptoms or damage compared to resistant plants. Intermediate resistant plants will usually show less severe symptoms or damage than susceptible plant varieties when grown under similar environmental conditions and/or specific disease(s) and or insect(s) pressure, but may have heavy damage under heavy pressure. Intermediate resistant bean plants are not immune to the disease(s) and or insect(s).

New Breeding Techniques: New breeding techniques are said of various new technologies developed and/or used to create new characteristics in plants through genetic variation, the aim being targeted mutagenesis, targeted introduction of new genes or gene silencing (RdDM). Example of such new breeding techniques are targeted sequence changes facilitated thru the use of Zinc finger nuclease (ZFN) technology (ZFN-1, ZFN-2 and ZFN-3, see U.S. Pat. No. 9,145,565, incorporated by reference in its entirety), Oligonucleotide directed mutagenesis (ODM), Cisgenesis and intragenesis, RNA-dependent DNA methylation (RdDM, which does not necessarily change nucleotide sequence but can change the biological activity of the sequence), Grafting (on GM rootstock), Reverse breeding, Agro-infiltration (agro-infiltration “sensu stricto”, agro-inoculation, floral dip), Transcription Activator-Like Effector Nucleases (TALENs, see U.S. Pat. Nos. 8,586,363 and 9,181,535, incorporated by reference in their entireties), the CRISPR/Cas system (see U.S. Pat. Nos. 8,697,359; 8,771,945; 8,795,965; 8,865,406; 8,871,445; 8,889,356; 8,895,308; 8,906,616; 8,932,814; 8,945,839; 8,993,233; and 8,999,641, which are all hereby incorporated by reference), engineered meganuclease, re-engineered homing endonucleases, DNA guided genome editing (Gao et al., Nature Biotechnology (2016), doi: 10.1038/nbt.3547, incorporated by reference in its entirety), and Synthetic genomics). A complete description of each of these techniques can be found in the report made by the Joint Research Center (JRC) Institute for Prospective Technological Studies of the European Commission in 2011 and titled “New plant breeding techniques—State-of-the-art and prospects for commercial development”, which is incorporated by reference in its entirety.

Machine harvestable bush. A machine harvestable bush means a bean plant that stands with pods off the ground. The pods can be removed by a machine from the plant without leaves and other plant parts.

Maturity. A maturity under 53 days is considered early while maturity between 54-59 days is considered average or medium and maturity of 60 or more days would be late.

Maturity date. Plants are considered mature when the pods have reached their maximum allowable seed size and sieve size for the specific use intended. This can vary for each end user, e.g., processing at different stages of maturity would be required for different types of consumer beans, such as “whole pack,” “cut,” or “french style.” The number of days is calculated from a relative planting date which depends on day length, heat units, and other environmental factors.

Plant adaptability. A plant having good plant adaptability means a plant that will perform well in different growing conditions and seasons.

Plant architecture. Plant architecture is the shape of the overall plant which can be tall narrow, short-wide, medium height, and/or medium width.

Plant cell. As used herein, the term “plant cell” includes plant cells whether isolated, in tissue culture, or incorporated in a plant or plant part.

Plant habit. A plant can be erect (upright) to sprawling on the ground.

Plant height. Plant height is taken from the top of the soil to the top node of the plant and is measured in centimeters or inches.

Plant part. As used herein, the term “plant part” includes any part of the plant including but not limited to leaves, stems, roots, seed, embryos, pollen, ovules, flowers, root tips, anthers, tissue, cells, pods, and the like.

Pod set height. The pod set height is the location of the pods within the plant. The pods can be high (near the top), low (near the bottom), or medium (in the middle) of the plant.

Regeneration. Regeneration refers to the development of a plant from tissue culture.

Resistance to disease(s) and or insect(s). A bean plant that restricts the growth and development of specific disease(s) and or insect(s) under normal disease(s) and or insect(s) attack pressure when compared to susceptible plants. These bean plants can exhibit some symptoms or damage under heavy disease(s) and or insect(s) pressure. Resistant bean plants are not immune to the disease(s) and or insect(s).

RHS. RHS refers to the Royal Horticultural Society of England which publishes an official botanical color chart quantitatively identifying colors according to a defined numbering system. The chart may be purchased from Royal Hort. Society Enterprise Ltd. RHS Garden; Wisley, Woking, Surrey GU236QB, UK.

Sieve size (sv). Sieve size 1 means pods that fall through a sieve grader which culls out pod diameters of 4.76 mm through 5.76 mm. Sieve size 2 means pods that fall through a sieve grader which culls out pod diameters of 5.76 mm through 7.34 mm. Sieve size 3 means pods that fall through a sieve grader which culls out pod diameters of 7.34 mm through 8.34 mm. Sieve size 4 means pods that fall through a sieve grader which culls out pod diameters of 8.34 mm through 9.53 mm. Sieve size 5 means pods that fall through a sieve grader which culls out pod diameters of 9.53 mm through 10.72 mm. Sieve size 6 means pods that fall through a sieve grader that will cull out pod diameters of 10.72 mm or larger.

Single gene converted (conversion). Single gene converted (conversion) plants refers to plants which are developed by a plant breeding technique called backcrossing wherein essentially all of the desired morphological and physiological characteristics of a variety are recovered in addition to the single gene transferred into the variety via the backcrossing technique or via genetic engineering. A single gene converted plant can also be referred to a plant obtained though mutagenesis or through the use of some new breeding techniques, whereas the single gene converted plant has essentially all of the desired morphological and physiological characteristics of the original variety in addition to the single gene muted or engineered through the new breeding techniques.

Slow seed development. Beans having slow seed development develop seed slowly even after the pods are full sized. This characteristic gives to the cultivar its field holding ability.

Susceptible to disease(s) and or insect(s). A bean plant that is susceptible to disease(s) and or insect(s) is defined as a bean plant that has the inability to restrict the growth and development of specific disease(s) and or insect(s). Plants that are susceptible will show damage when infected and are more likely to have heavy damage under moderate levels of specific disease(s) and or insect(s).

Tolerance to abiotic stresses. A bean plant that is tolerant to abiotic stresses has the ability to endure abiotic stress without serious consequences for growth, appearance and yield.

Uniformity. Uniformity, as used herein, describes the similarity between plants or plant characteristics which can be a described by qualitative or quantitative measurements.

Variety. A plant variety as used by one skilled in the art of plant breeding means a plant grouping within a single botanical taxon of the lowest known rank which can be defined by the expression of the characteristics resulting from a given genotype or combination of phenotypes, distinguished from any other plant grouping by the expression of at least one of the said characteristics and considered as a unit with regard to its suitability for being propagated unchanged (International convention for the protection of new varieties of plants).

There are numerous steps in the development of any novel, desirable plant germplasm. Plant breeding begins with the analysis and definition of problems and weaknesses of the current germplasm, the establishment of program goals, and the definition of specific breeding objectives. The next step is selection of germplasm that possesses the traits to meet the program goals. The goal is to combine in a single variety or hybrid an improved combination of desirable traits from the parental germplasm.

In garden bean, these important traits may include increased fresh pod yield, higher seed yield, improved color, resistance to diseases and insects, better stems and roots, tolerance to drought and heat, better standing ability in the field, better uniformity, and better agronomic quality. With mechanical harvesting of many crops, uniformity of plant characteristics such as germination and stand establishment, growth rate, maturity and plant height is important.

In some embodiments, particularly desirable traits that may be incorporated by this invention are improved resistance to different viral, fungal, and bacterial pathogens. Important diseases include but are not limited to fungi such as Uromyces appendiculatus (rust), Colletotrichum lindemuthianum (anthracnose), virus such as BCMV (bean common mosaic virus), BCTV (bean curly top virus), bacteria such as Pseudomonas (Pseudomonas savastanoi pv. Phaseolicola (halo blight), Pseudomonas syringae pv. Syringae (bacterial brown spot)) or Xanthomonas (Xanthomonas axonopodis pv. Phaseoli (common blight). Improved resistance to insect pests is another desirable trait that may be incorporated into new garden plants developed by this invention.

Bean Breeding

The goal of bean breeding is to develop new, unique and superior garden bean cultivar and hybrids. The breeder initially selects and crosses two or more parental lines, followed by repeated selfing and selection, producing many new genetic combinations. Another method used to develop new, unique and superior garden bean cultivar occurs when the breeder selects and crosses two or more parental lines followed by haploid induction and chromosome doubling that result in the development of dihaploid cultivars. The breeder can theoretically generate billions of different genetic combinations via crossing, selfing and mutations and the same is true for the utilization of the dihaploid breeding method.

Each year, the plant breeder selects the germplasm to advance to the next generation. This germplasm is grown under unique and different geographical, climatic and soil conditions, and further selections are then made, during and at the end of the growing season. The cultivars developed are unpredictable. This unpredictability is because the breeder's selection occurs in unique environments, with no control at the DNA level (using conventional breeding procedures or dihaploid breeding procedures), and with millions of different possible genetic combinations being generated. A breeder of ordinary skill in the art cannot predict the final resulting cultivars he develops, except possibly in a very gross and general fashion. This unpredictability results in the expenditure of large research monies to develop superior new garden bean cultivars.

The development of commercial garden bean cultivar requires the development and selection of garden bean plants, the crossing of these plants, and the evaluation of the crosses.

Pedigree breeding and recurrent selection breeding methods are used to develop cultivars from breeding populations. Breeding programs combine desirable traits from two or more cultivars or various broad-based sources into breeding pools from which cultivars are developed by selfing and selection of desired phenotypes or through the dihaploid breeding method followed by the selection of desired phenotypes. The new cultivars are evaluated to determine which have commercial potential.

Choice of breeding or selection methods depends on the mode of plant reproduction, the heritability of the trait(s) being improved, and the type of cultivar used commercially (e.g., F₁ hybrid cultivar, pureline cultivar, etc.). For highly heritable traits, a choice of superior individual plants evaluated at a single location will be effective, whereas for traits with low heritability, selection should be based on mean values obtained from replicated evaluations of families of related plants. Popular selection methods commonly include pedigree selection, modified pedigree selection, mass selection, recurrent selection, and backcross breeding.

i. Pedigree Selection

Pedigree breeding is used commonly for the improvement of self-pollinating crops or inbred lines of cross-pollinating crops. Two parents possessing favorable, complementary traits are crossed to produce an F₁. An F₂ population is produced by selfing one or several F₁s or by intercrossing two F₁s (sib mating). The dihaploid breeding method could also be used. Selection of the best individuals is usually begun in the F₂ population; then, beginning in the F₃, the best individuals in the best families are selected. Replicated testing of families, or hybrid combinations involving individuals of these families, often follows in the F₄ generation to improve the effectiveness of selection for traits with low heritability. At an advanced stage of inbreeding (i.e., F₆ and F₇), the best lines or mixtures of phenotypically similar lines are tested for potential release of new cultivars. Similarly, the development of new cultivars through the dihaploid system requires the selection of the cultivars followed by two to five years of testing in replicated plots.

ii. Backcross Breeding

Backcross breeding has been used to transfer genes for a simply inherited, highly heritable trait into a desirable homozygous cultivar or inbred line which is the recurrent parent. The source of the trait to be transferred is called the donor parent. The resulting plant is expected to have the attributes of the recurrent parent (e.g., cultivar) and the desirable trait transferred from the donor parent. After the initial cross, individuals possessing the phenotype of the donor parent are selected and repeatedly crossed (backcrossed) to the recurrent parent. The resulting plant is expected to have the attributes of the recurrent parent (e.g., cultivar) and the desirable trait transferred from the donor parent.

When the term garden bean cultivar is used in the context of the present invention, this also includes any garden bean cultivar plant where one or more desired trait has been introduced through backcrossing methods, whether such trait is a naturally occurring one, a mutant, a gene or a nucleotide sequence modified by the use of New Breeding Techniques. Backcrossing methods can be used with the present invention to improve or introduce one or more characteristic into the garden bean cultivar of the present invention. The term “backcrossing” as used herein refers to the repeated crossing of a hybrid progeny back to the recurrent parent, i.e., backcrossing one, two, three, four, five, six, seven, eight, nine, or more times to the recurrent parent. The parental garden bean cultivar plant which contributes the gene or the genes for the desired characteristic is termed the nonrecurrent or donor parent. This terminology refers to the fact that the nonrecurrent parent is used one time in the backcross protocol and therefore does not recur. The parental garden bean cultivar to which the gene or genes from the nonrecurrent parent are transferred is known as the recurrent parent as it is used for several rounds in the backcrossing protocol.

In a typical backcross protocol, the original cultivar of interest (recurrent parent) is crossed to a second cultivar (nonrecurrent parent) that carries the gene or genes of interest to be transferred. The resulting progeny from this cross are then crossed again to the recurrent parent and the process is repeated until a garden bean plant is obtained wherein all the desired morphological and physiological characteristics of the recurrent parent are recovered in the converted plant, generally determined at a 5% significance level when grown in the same environmental conditions, in addition to the gene or genes transferred from the nonrecurrent parent. It has to be noted that some, one, two, three or more, self-pollination and growing of population might be included between two successive backcrosses. Indeed, an appropriate selection in the population produced by the self-pollination, i.e. selection for the desired trait and physiological and morphological characteristics of the recurrent parent might be equivalent to one, two or even three additional backcrosses in a continuous series without rigorous selection, saving then time, money and effort to the breeder. A non-limiting example of such a protocol would be the following: a) the first generation F1 produced by the cross of the recurrent parent A by the donor parent B is backcrossed to parent A, b) selection is practiced for the plants having the desired trait of parent B, c) selected plant are self-pollinated to produce a population of plants where selection is practiced for the plants having the desired trait of parent B and physiological and morphological characteristics of parent A, d) the selected plants are backcrossed one, two, three, four, five, six, seven, eight, nine, or more times to parent A to produce selected backcross progeny plants comprising the desired trait of parent B and the physiological and morphological characteristics of parent A. Step (c) may or may not be repeated and included between the backcrosses of step (d).

The selection of a suitable recurrent parent is an important step for a successful backcrossing procedure. The goal of a backcross protocol is to alter or substitute one or more trait(s) or characteristic(s) in the original inbred parental line in order to find it then in the hybrid made thereof. To accomplish this, a gene or genes of the recurrent inbred is modified or substituted with the desired gene or genes from the nonrecurrent parent, while retaining essentially all of the rest of the desired genetic, and therefore the desired physiological and morphological, constitution of the original inbred. The choice of the particular nonrecurrent parent will depend on the purpose of the backcross; one of the major purposes is to add some commercially desirable, agronomically important trait(s) to the plant. The exact backcrossing protocol will depend on the characteristic(s) or trait(s) being altered to determine an appropriate testing protocol. Although backcrossing methods are simplified when the characteristic being transferred is a single gene and dominant allele, multiple genes and recessive allele(s) may also be transferred and therefore, backcross breeding is by no means restricted to character(s) governed by one or a few genes. In fact the number of genes might be less important that the identification of the character(s) in the segregating population. In this instance it may then be necessary to introduce a test of the progeny to determine if the desired characteristic(s) has been successfully transferred. Such tests encompass visual inspection, simple crossing, but also follow up of the characteristic(s) through genetically associated markers and molecular assisted breeding tools. For example, selection of progeny containing the transferred trait is done by direct selection, visual inspection for a trait associated with a dominant allele, while the selection of progeny for a trait that is transferred via a recessive allele, such as the waxy starch characteristic in corn, require selfing the progeny to determine which plant carry the recessive allele(s).

Many single gene traits have been identified that are not regularly selected for in the development of a new parental inbred of a hybrid garden bean plant according to the invention but that can be improved by backcrossing techniques. Examples of these traits include but are not limited to herbicide resistance (such as bar or pat genes), resistance for bacterial, fungal, or viral disease (such as gene I used for BCMV resistance), insect resistance, enhanced nutritional quality (such as 2s albumine gene), industrial usage, agronomic qualities (such as the “persistent green gene”), yield stability, and yield enhancement. Many single gene traits have been identified that are not regularly selected for in the development of a new line but that can be improved by backcrossing techniques. These genes are generally inherited through the nucleus. Some other single gene traits are described in U.S. Pat. Nos. 5,777,196, 5,948,957, and 5,969,212, the disclosures of which are specifically hereby incorporated by reference.

In 1981, the backcross method of breeding counted for 17% of the total breeding effort for inbred line development in the United States, accordingly to, Hallauer, A. R. et al. (1988) “Corn Breeding” Corn and Corn Improvement, No. 18, pp. 463-481.

The backcross breeding method provides a precise way of improving varieties that excel in a large number of attributes but are deficient in a few characteristics. (Page 150 of the Pr. R. W. Allard's 1960 book, published by John Wiley & Sons, Inc, Principles of Plant Breeding). The method makes use of a series of backcrosses to the variety to be improved during which the character or the characters in which improvement is sought is maintained by selection. At the end of the backcrossing the gene or genes being transferred unlike all other genes, will be heterozygous. Selfing after the last backcross produces homozygosity for this gene pair(s) and, coupled with selection, will result in a parental line of a hybrid variety with exactly the adaptation, yielding ability and quality characteristics of the recurrent parent but superior to that parent in the particular characteristic(s) for which the improvement program was undertaken. Therefore, this method provides the plant breeder with a high degree of genetic control of his work.

The method is scientifically exact because the morphological and agricultural features of the improved variety could be described in advance and because the same variety could, if it were desired, be bred a second time by retracing the same steps (Briggs, “Breeding wheats resistant to bunt by the backcross method”, 1930 Jour. Amer. Soc. Agron., 22: 289-244).

Backcrossing is a powerful mechanism for achieving homozygosity and any population obtained by backcrossing must rapidly converge on the genotype of the recurrent parent. When backcrossing is made the basis of a plant breeding program, the genotype of the recurrent parent will be modified only with regards to genes being transferred, which are maintained in the population by selection.

Successful backcrosses are, for example, the transfer of stem rust resistance from ‘Hope’ wheat to ‘Bart wheat’ and even pursuing the backcrosses with the transfer of bunt resistance to create ‘Bart 38’, having both resistances. Also highlighted by Allard is the successful transfer of mildew, leaf spot and wilt resistances in California Common alfalfa to create ‘Caliverde’. This new ‘Caliverde’ variety produced through the backcross process is indistinguishable from California Common except for its resistance to the three named diseases.

One of the advantages of the backcross method is that the breeding program can be carried out in almost every environment that will allow the development of the character being transferred.

The backcross technique is not only desirable when breeding for disease resistance but also for the adjustment of morphological characters, colour characteristics and simply inherited quantitative characters such as earliness, plant height and seed size and shape. In this regard, a medium grain type variety, ‘Calady’, has been produced by Jones and Davis. As dealing with quantitative characteristics, they selected the donor parent with the view of sacrificing some of the intensity of the character for which it was chosen, i.e. grain size. ‘Lady Wright’, a long grain variety was used as the donor parent and ‘Coloro’, a short grain one as the recurrent parent. After four backcrosses, the medium grain type variety ‘Calady’ was produced.

iii. Single-Seed Descent and Multiple Seed Procedures

The single-seed descent procedure in the strict sense refers to planting a segregating population, harvesting a sample of one seed per plant, and using the one-seed sample to plant the next generation. When the population has been advanced from the F2 to the desired level of inbreeding, the plants from which lines are derived will each trace to different F2 individuals. The number of plants in a population declines each generation due to failure of some seeds to germinate or some plants to produce at least one seed. As a result, not all of the F2 plants originally sampled in the population will be represented by a progeny when generation advance is completed.

In a multiple-seed procedure, breeders commonly harvest one or more flower containing seed from each plant in a population and blend them together to form a bulk seed lot. Part of the bulked seed is used to plant the next generation and part is put in reserve. The procedure has been referred to as modified single-seed descent or the bulk technique.

The multiple-seed procedure has been used to save labor at harvest. It is considerably faster than removing one seed from each flower by hand for the single seed procedure. The multiple-seed procedure also makes it possible to plant the same number of seeds of a population each generation of inbreeding. Enough seeds are harvested to make up for those plants that did not germinate or produce seed.

Descriptions of other breeding methods that are commonly used for different traits and crops can be found in one of several reference books (e.g., R. W. Allard, 1960, Principles of Plant Breeding, John Wiley and Son, pp. 115-161; N. W. Simmonds, 1979, Principles of Crop Improvement, Longman Group Limited; W. R. Fehr, 1987, Principles of Crop Development, Macmillan Publishing Co.; N. F. Jensen, 1988, Plant Breeding Methodology, John Wiley & Sons).

iv. Open-Pollinated Populations

The improvement of open-pollinated populations of such crops as rye, maize and sugar beets, herbage grasses, legumes such as alfalfa and clover, and tropical tree crops such as cacao, coconuts, oil palm and some rubber, depends essentially upon changing gene-frequencies towards fixation of favorable alleles while maintaining a high (but far from maximal) degree of heterozygosity.

Uniformity in such populations is impossible and trueness-to-type in an open-pollinated variety is a statistical feature of the population as a whole, not a characteristic of individual plants. Thus, the heterogeneity of open-pollinated populations contrasts with the homogeneity (or virtually so) of inbred lines, clones and hybrids.

Population improvement methods fall naturally into two groups, those based on purely phenotypic selection, normally called mass selection, and those based on selection with progeny testing. Interpopulation improvement utilizes the concept of open breeding populations; allowing genes to flow from one population to another. Plants in one population (cultivar, strain, ecotype, or any germplasm source) are crossed either naturally (e.g., by wind) or by hand or by bees (commonly Apis mellifera L. or Megachile rotundata F.) with plants from other populations. Selection is applied to improve one (or sometimes both) population(s) by isolating plants with desirable traits from both sources.

There are basically two primary methods of open-pollinated population improvement.

First, there is the situation in which a population is changed en masse by a chosen selection procedure. The outcome is an improved population that is indefinitely propagable by random-mating within itself in isolation.

Second, the synthetic variety attains the same end result as population improvement, but is not itself propagable as such; it has to be reconstructed from parental lines or clones. These plant breeding procedures for improving open-pollinated populations are well known to those skilled in the art and comprehensive reviews of breeding procedures routinely used for improving cross-pollinated plants are provided in numerous texts and articles, including: Allard, Principles of Plant Breeding, John Wiley & Sons, Inc. (1960); Simmonds, Principles of Crop Improvement, Longman Group Limited (1979); Hallauer and Miranda, Quantitative Genetics in Maize Breeding, Iowa State University Press (1981); and, Jensen, Plant Breeding Methodology, John Wiley & Sons, Inc. (1988).

A) Mass Selection

Mass and recurrent selections can be used to improve populations of either self- or cross-pollinating crops. A genetically variable population of heterozygous individuals is either identified or created by intercrossing several different parents. The best plants are selected based on individual superiority, outstanding progeny, or excellent combining ability. The selected plants are intercrossed to produce a new population in which further cycles of selection are continued. In mass selection, desirable individual plants are chosen, harvested, and the seed composited without progeny testing to produce the following generation. Since selection is based on the maternal parent only, and there is no control over pollination, mass selection amounts to a form of random mating with selection. As stated above, the purpose of mass selection is to increase the proportion of superior genotypes in the population.

B) Synthetics

A synthetic variety is produced by crossing inter se a number of genotypes selected for good combining ability in all possible hybrid combinations, with subsequent maintenance of the variety by open pollination. Whether parents are (more or less inbred) seed-propagated lines, as in some sugar beet and beans (Vicia) or clones, as in herbage grasses, clovers and alfalfa, makes no difference in principle. Parents are selected on general combining ability, sometimes by test crosses or toperosses, more generally by polycrosses. Parental seed lines may be deliberately inbred (e.g. by selfing or sib crossing). However, even if the parents are not deliberately inbred, selection within lines during line maintenance will ensure that some inbreeding occurs. Clonal parents will, of course, remain unchanged and highly heterozygous.

Whether a synthetic can go straight from the parental seed production plot to the farmer or must first undergo one or more cycles of multiplication depends on seed production and the scale of demand for seed. In practice, grasses and clovers are generally multiplied once or twice and are thus considerably removed from the original synthetic.

While mass selection is sometimes used, progeny testing is generally preferred for polycrosses, because of their operational simplicity and obvious relevance to the objective, namely exploitation of general combining ability in a synthetic.

The number of parental lines or clones that enters a synthetic varies widely. In practice, numbers of parental lines range from 10 to several hundred, with 100-200 being the average. Broad based synthetics formed from 100 or more clones would be expected to be more stable during seed multiplication than narrow based synthetics.

v. Hybrids

A hybrid is an individual plant resulting from a cross between parents of differing genotypes. Commercial hybrids are now used extensively in many crops, including corn (maize), sorghum, sugar beet, sunflower and broccoli. Hybrids can be formed in a number of different ways, including by crossing two parents directly (single cross hybrids), by crossing a single cross hybrid with another parent (three-way or triple cross hybrids), or by crossing two different hybrids (four-way or double cross hybrids).

Strictly speaking, most individuals in an out breeding (i.e., open-pollinated) population are hybrids, but the term is usually reserved for cases in which the parents are individuals whose genomes are sufficiently distinct for them to be recognized as different species or subspecies. Hybrids may be fertile or sterile depending on qualitative and/or quantitative differences in the genomes of the two parents. Heterosis, or hybrid vigor, is usually associated with increased heterozygosity that results in increased vigor of growth, survival, and fertility of hybrids as compared with the parental lines that were used to form the hybrid. Maximum heterosis is usually achieved by crossing two genetically different, highly inbred lines.

Once the inbreds that give the best hybrid performance have been identified, the hybrid seed can be reproduced indefinitely as long as the homogeneity of the inbred parent is maintained. A single-cross hybrid is produced when two inbred lines are crossed to produce the F1 progeny. A double-cross hybrid is produced from four inbred lines crossed in pairs (A×B and C×D) and then the two F1 hybrids are crossed again (A×B)×(C×D). Much of the hybrid vigor and uniformity exhibited by F1 hybrids is lost in the next generation (F2). Consequently, seed from F2 hybrid varieties is not used for planting stock.

The production of hybrids is a well-developed industry, involving the isolated production of both the parental lines and the hybrids which result from crossing those lines. For a detailed discussion of the hybrid production process, see, e.g., Wright, Commercial Hybrid Seed Production 8:161-176, In Hybridization of Crop Plants.

vi. Bulk Segregation Analysis (BSA)

BSA, a.k.a. bulked segregation analysis, or bulk segregant analysis, is a method described by Michelmore et al. (Michelmore et al., 1991, Identification of markers linked to disease-resistance genes by bulked segregant analysis: a rapid method to detect markers in specific genomic regions by using segregating populations. Proceedings of the National Academy of Sciences, USA, 99:9828-9832) and Quarrie et al. (Quarrie et al., 1999, Journal of Experimental Botany, 50(337):1299-1306).

For BSA of a trait of interest, parental lines with certain different phenotypes are chosen and crossed to generate F2, doubled haploid or recombinant inbred populations with QTL analysis. The population is then phenotyped to identify individual plants or lines having high or low expression of the trait. Two DNA bulks are prepared, one from the individuals having one phenotype (e.g., resistant to virus), and the other from the individuals having reversed phenotype (e.g., susceptible to virus), and analyzed for allele frequency with molecular markers. Only a few individuals are required in each bulk (e.g., 10 plants each) if the markers are dominant (e.g., RAPDs). More individuals are needed when markers are co-dominant (e.g., RFLPs). Markers linked to the phenotype can be identified and used for breeding or QTL mapping.

vii. Hand-Pollination Method

Hand pollination describes the crossing of plants via the deliberate fertilization of female ovules with pollen from a desired male parent plant. In some embodiments the donor or recipient female parent and the donor or recipient male parent line are planted in the same field. In some embodiments the donor or recipient female parent and the donor or recipient male parent line are planted in the same greenhouse. The inbred male parent can be planted earlier than the female parent to ensure adequate pollen supply at the pollination time. In some embodiments, the male parent and female parent can be planted at a ratio of 1 male parent to 4-10 female parents. Pollination is started when the female parent flower is ready to be fertilized. Female flower buds that are ready to open in the following days are identified, covered with paper cups or small paper bags that prevent bee or any other insect from visiting the female flowers, and marked with any kind of material that can be easily seen the next morning. The male flowers of the male parent are collected in the early morning before they are open and visited by pollinating insects. The covered female flowers of the female parent, which have opened, are un-covered and pollinated with the collected fresh male flowers of the male parent, starting as soon as the male flower sheds pollen. The pollinated female flowers are again covered after pollination to prevent bees and any other insects visit. The pollinated female flowers are also marked. The marked flowers are harvested. In some embodiments, the male pollen used for fertilization has been previously collected and stored.

viii. Bee-Pollination Method

Using the bee-pollination method, the parent plants are usually planted within close proximity. In some embodiments more female plants are planted to allow for a greater production of seed. Insects are placed in the field or greenhouses for transfer of pollen from the male parent to the female flowers of the female parent.

ix. Targeting Induced Local Lesions in Genomes (TILLING)

Breeding schemes of the present application can include crosses with TILLING® plant cultivars. TILLING® is a method in molecular biology that allows directed identification of mutations in a specific gene. TILLING® was introduced in 2000, using the model plant Arabidopsis thaliana. TILLING® has since been used as a reverse genetics method in other organisms such as zebrafish, corn, wheat, rice, soybean, tomato and lettuce.

The method combines a standard and efficient technique of mutagenesis with a chemical mutagen (e.g., Ethyl methanesulfonate (EMS)) with a sensitive DNA screening-technique that identifies single base mutations (also called point mutations) in a target gene. EcoTILLING is a method that uses TILLING® techniques to look for natural mutations in individuals, usually for population genetics analysis (see Comai, et al., 2003 The Plant Journal 37, 778-786; Gilchrist et al. 2006 Mol. Ecol. 15, 1367-1378; Mejlhede et al. 2006 Plant Breeding 125, 461-467; Nieto et al. 2007 BMC Plant Biology 7, 34-42, each of which is incorporated by reference hereby for all purposes). DEcoTILLING is a modification of TILLING® and EcoTILLING which uses an inexpensive method to identify fragments (Garvin et al., 2007, DEco-TILLING: An inexpensive method for SNP discovery that reduces ascertainment bias. Molecular Ecology Notes 7, 735-746).

The TILLING® method relies on the formation of heteroduplexes that are formed when multiple alleles (which could be from a heterozygote or a pool of multiple homozygotes and heterozygotes) are amplified in a PCR, heated, and then slowly cooled. A “bubble” forms at the mismatch of the two DNA strands (the induced mutation in TILLING® or the natural mutation or SNP in EcoTILLING), which is then cleaved by single stranded nucleases. The products are then separated by size on several different platforms.

Several TILLING® centers exists over the world that focus on agriculturally important species: UC Davis (USA), focusing on Rice; Purdue University (USA), focusing on Maize; University of British Columbia (CA), focusing on Brassica napus; John Innes Centre (UK), focusing on Brassica rapa; Fred Hutchinson Cancer Research, focusing on Arabidopsis; Southern Illinois University (USA), focusing on Soybean; John Innes Centre (UK), focusing on Lotus and Medicago; and INRA (France), focusing on Pea and Tomato.

More detailed description on methods and compositions on TILLING® can be found in U.S. Pat. No. 5,994,075, US 2004/0053236 A1, WO 2005/055704, and WO 2005/048692, each of which is hereby incorporated by reference for all purposes.

Thus in some embodiments, the breeding methods of the present disclosure include breeding with one or more TILLING plant lines with one or more identified mutations.

x. Mutation Breeding

Mutation breeding is another method of introducing new traits into garden bean plants. Mutations that occur spontaneously or are artificially induced can be useful sources of variability for a plant breeder. The goal of artificial mutagenesis is to increase the rate of mutation for a desired characteristic. Mutation rates can be increased by many different means or mutating agents including temperature, long-term seed storage, tissue culture conditions, radiation (such as X-rays, Gamma rays, neutrons, Beta radiation, or ultraviolet radiation), chemical mutagens (such as base analogs like 5-bromo-uracil), antibiotics, alkylating agents (such as sulfur mustards, nitrogen mustards, epoxides, ethyleneamines, sulfates, sulfonates, sulfones, or lactones), azide, hydroxylamine, nitrous acid or acridines. Once a desired trait is observed through mutagenesis the trait may then be incorporated into existing germplasm by traditional breeding techniques. Details of mutation breeding can be found in W. R. Fehr, 1993, Principles of Cultivar Development, Macmillan Publishing Co.

New breeding techniques such as the ones involving the uses of Zinc Finger Nucleases or oligonucleotide directed mutagenesis shall also be used to generate genetic variability and introduce new traits into garden bean varieties.

xi. Double Haploids and Chromosome Doubling

One way to obtain homozygous plants without the need to cross two parental lines followed by a long selection of the segregating progeny, and/or multiple back-crossings is to produce haploids and then double the chromosomes to form doubled haploids. Haploid plants can occur spontaneously, or may be artificially induced via chemical treatments or by crossing plants with inducer lines (Seymour et al. 2012, PNAS vol 109, pg 4227-4232; Zhang et al., 2008 Plant Cell Rep. December 27(12) 1851-60). The production of haploid progeny can occur via a variety of mechanisms which can affect the distribution of chromosomes during gamete formation. The chromosome complements of haploids sometimes double spontaneously to produce homozygous doubled haploids (DHs). Mixoploids, which are plants which contain cells having different ploidies, can sometimes arise and may represent plants that are undergoing chromosome doubling so as to spontaneously produce doubled haploid tissues, organs, shoots, floral parts or plants. Another common technique is to induce the formation of double haploid plants with a chromosome doubling treatment such as colchicine (El-Hennawy et al., 2011 Vol 56, issue 2 pg 63-72; Doubled Haploid Production in Crop Plants 2003 edited by Maluszynski ISBN 1-4020-1544-5). The production of doubled haploid plants yields highly uniform cultivars and is especially desirable as an alternative to sexual inbreeding of longer-generation crops. By producing doubled haploid progeny, the number of possible gene combinations for inherited traits is more manageable. Thus, an efficient doubled haploid technology can significantly reduce the time and the cost of inbred and cultivar development.

xii. Protoplast Fusion

In another method for breeding plants, protoplast fusion can also be used for the transfer of trait-conferring genomic material from a donor plant to a recipient plant. Protoplast fusion is an induced or spontaneous union, such as a somatic hybridization, between two or more protoplasts (cells of which the cell walls are removed by enzymatic treatment) to produce a single bi- or multi-nucleate cell. The fused cell that may even be obtained with plant species that cannot be interbred in nature is tissue cultured into a hybrid plant exhibiting the desirable combination of traits.

xiii. Embryo Rescue

Alternatively, embryo rescue may be employed in the transfer of resistance-conferring genomic material from a donor plant to a recipient plant. Embryo rescue can be used as a procedure to isolate embryo's from crosses wherein plants fail to produce viable seed. In this process, the fertilized ovary or immature seed of a plant is tissue cultured to create new plants (see Pierik, 1999, In vitro culture of higher plants, Springer, ISBN 079235267x, 9780792352679, which is incorporated herein by reference in its entirety).

Breeding Evaluation

Each breeding program can include a periodic, objective evaluation of the efficiency of the breeding procedure. Evaluation criteria vary depending on the goal and objectives, but should include gain from selection per year based on comparisons to an appropriate standard, overall value of the advanced breeding lines, and number of successful cultivars produced per unit of input (e.g., per year, per dollar expended, etc.).

Promising advanced breeding lines are thoroughly tested per se and in hybrid combination and compared to appropriate standards in environments representative of the commercial target area(s). The best lines are candidates for use as parents in new commercial cultivars; those still deficient in a few traits may be used as parents to produce new populations for further selection.

In one embodiment, the plants are selected on the basis of one or more phenotypic traits. Skilled persons will readily appreciate that such traits include any observable characteristic of the plant, including for example growth rate, height, weight, color, taste, smell, changes in the production of one or more compounds by the plant (including for example, metabolites, proteins, drugs, carbohydrates, oils, and any other compounds).

A most difficult task is the identification of individuals that are genetically superior, because for most traits the true genotypic value is masked by other confounding plant traits or environmental factors. One method of identifying a superior plant is to observe its performance relative to other experimental plants and to a widely grown standard cultivar. If a single observation is inconclusive, replicated observations provide a better estimate of its genetic worth.

Proper testing should detect any major faults and establish the level of superiority or improvement over current cultivars. In addition to showing superior performance, there must be a demand for a new cultivar that is compatible with industry standards or which creates a new market. The introduction of a new cultivar will incur additional costs to the seed producer, the grower, processor and consumer; for special advertising and marketing, altered seed and commercial production practices, and new product utilization. The testing preceding release of a new cultivar should take into consideration research and development costs as well as technical superiority of the final cultivar. For seed-propagated cultivars, it must be feasible to produce seed easily and economically.

It should be appreciated that in certain embodiments, plants may be selected based on the absence, suppression or inhibition of a certain feature or trait (such as an undesirable feature or trait) as opposed to the presence of a certain feature or trait (such as a desirable feature or trait).

Selecting plants based on genotypic information is also envisaged (for example, including the pattern of plant gene expression, genotype, or presence of genetic markers). Where the presence of one or more genetic marker is assessed, the one or more marker may already be known and/or associated with a particular characteristic of a plant; for example, a marker or markers may be associated with an increased growth rate or metabolite profile. This information could be used in combination with assessment based on other characteristics in a method of the disclosure to select for a combination of different plant characteristics that may be desirable. Such techniques may be used to identify novel quantitative trait loci (QTLs). By way of example, plants may be selected based on growth rate, size (including but not limited to weight, height, leaf size, stem size, branching pattern, or the size of any part of the plant), general health, survival, tolerance to adverse physical environments and/or any other characteristic, as described herein before.

Further non-limiting examples include selecting plants based on: speed of seed germination; quantity of biomass produced; increased root, and/or leaf/shoot growth that leads to an increased yield (herbage or grain or fiber or oil) or biomass production; effects on plant growth that results in an increased seed yield for a crop; effects on plant growth which result in an increased head yield; effects on plant growth that lead to an increased resistance or tolerance disease including fungal, viral or bacterial diseases or to pests such as insects, mites or nematodes in which damage is measured by decreased foliar symptoms such as the incidence of bacterial or fungal lesions, or area of damaged foliage or reduction in the numbers of nematode cysts or galls on plant roots, or improvements in plant yield in the presence of such plant pests and diseases; effects on plant growth that lead to increased metabolite yields; effects on plant growth that lead to improved aesthetic appeal which may be particularly important in plants grown for their form, color or taste, for example the color intensity of garden bean leaves, or the taste of said leaves.

Molecular Breeding Evaluation Techniques

Selection of plants based on phenotypic or genotypic information may be performed using techniques such as, but not limited to: high through-put screening of chemical components of plant origin, sequencing techniques including high through-put sequencing of genetic material, differential display techniques (including DDRT-PCR, and DD-PCR), nucleic acid microarray techniques, RNA-seq (Whole Transcriptome Shotgun Sequencing), qRTPCR (quantitative real time PCR).

In one embodiment, the evaluating step of a plant breeding program involves the identification of desirable traits in progeny plants. Progeny plants can be grown in, or exposed to conditions designed to emphasize a particular trait (e.g. drought conditions for drought tolerance, lower temperatures for freezing tolerant traits). Progeny plants with the highest scores for a particular trait may be used for subsequent breeding steps.

In some embodiments, plants selected from the evaluation step can exhibit a 1%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 100%, 120% or more improvement in a particular plant trait compared to a control plant.

In other embodiments, the evaluating step of plant breeding comprises one or more molecular biological tests for genes or other markers. For example, the molecular biological test can involve probe hybridization and/or amplification of nucleic acid (e.g., measuring nucleic acid density by Northern or Southern hybridization, PCR) and/or immunological detection (e.g., measuring protein density, such as precipitation and agglutination tests, ELISA (e.g., Lateral Flow test or DAS-ELISA), Western blot, RIA, immune labeling, immunosorbent electron microscopy (ISEM), and/or dot blot).

The procedure to perform a nucleic acid hybridization, an amplification of nucleic acid (e.g., RT-PCR) or an immunological detection (e.g., precipitation and agglutination tests, ELISA (e.g., Lateral Flow test or DAS-ELISA), Western blot, RIA, immunogold or immunofluorescent labeling, immunosorbent electron microscopy (ISEM), and/or dot blot tests) are performed as described elsewhere herein and well-known by one skilled in the art.

In one embodiment, the evaluating step comprises PCR (semi-quantitative or quantitative), wherein primers are used to amplify one or more nucleic acid sequences of a desirable gene, or a nucleic acid associated with said gene or a desirable trait (e.g., a co-segregating nucleic acid, or other marker).

In another embodiment, the evaluating step comprises immunological detection (e.g., precipitation and agglutination tests, ELISA (e.g., Lateral Flow test or DAS-ELISA), Western blot, RIA, immuno labeling (gold, fluorescent, or other detectable marker), immunosorbent electron microscopy (ISEM), and/or dot blot), wherein one or more gene or marker-specific antibodies are used to detect one or more desirable proteins. In one embodiment, said specific antibody is selected from the group consisting of polyclonal antibodies, monoclonal antibodies, antibody fragments, and combination thereof.

Reverse Transcription Polymerase Chain Reaction (RT-PCR) can be utilized in the present disclosure to determine expression of a gene to assist during the selection step of a breeding scheme. It is a variant of polymerase chain reaction (PCR), a laboratory technique commonly used in molecular biology to generate many copies of a DNA sequence, a process termed “amplification”. In RT-PCR, however, RNA strand is first reverse transcribed into its DNA complement (complementary DNA, or cDNA) using the enzyme reverse transcriptase, and the resulting cDNA is amplified using traditional or real-time PCR.

RT-PCR utilizes a pair of primers, which are complementary to a defined sequence on each of the two strands of the cDNA. These primers are then extended by a DNA polymerase and a copy of the strand is made after each cycle, leading to logarithmic amplification.

RT-PCR includes three major steps. The first step is the reverse transcription (RT) where RNA is reverse transcribed to cDNA using a reverse transcriptase and primers. This step is very important in order to allow the performance of PCR since DNA polymerase can act only on DNA templates. The RT step can be performed either in the same tube with PCR (one-step PCR) or in a separate one (two-step PCR) using a temperature between 40° C. and 50° C., depending on the properties of the reverse transcriptase used.

The next step involves the denaturation of the dsDNA at 95° C., so that the two strands separate and the primers can bind again at lower temperatures and begin a new chain reaction. Then, the temperature is decreased until it reaches the annealing temperature which can vary depending on the set of primers used, their concentration, the probe and its concentration (if used), and the cations concentration. The main consideration, of course, when choosing the optimal annealing temperature is the melting temperature (Tm) of the primers and probes (if used). The annealing temperature chosen for a PCR depends directly on length and composition of the primers. This is the result of the difference of hydrogen bonds between A-T (2 bonds) and G-C (3 bonds). An annealing temperature about 5 degrees below the lowest Tm of the pair of primers is usually used.

The final step of PCR amplification is the DNA extension from the primers which is done by the thermostable Taq DNA polymerase usually at 72° C., which is the optimal temperature for the polymerase to work. The length of the incubation at each temperature, the temperature alterations and the number of cycles are controlled by a programmable thermal cycler. The analysis of the PCR products depends on the type of PCR applied. If a conventional PCR is used, the PCR product is detected using agarose gel electrophoresis and ethidium bromide (or other nucleic acid staining).

Conventional RT-PCR is a time-consuming technique with important limitations when compared to real time PCR techniques. This, combined with the fact that ethidium bromide has low sensitivity, yields results that are not always reliable. Moreover, there is an increased cross-contamination risk of the samples since detection of the PCR product requires the post-amplification processing of the samples. Furthermore, the specificity of the assay is mainly determined by the primers, which can give false-positive results. However, the most important issue concerning conventional RT-PCR is the fact that it is a semi or even a low quantitative technique, where the amplicon can be visualized only after the amplification ends.

Real time RT-PCR provides a method where the amplicons can be visualized as the amplification progresses using a fluorescent reporter molecule. There are three major kinds of fluorescent reporters used in real time RT-PCR, general non specific DNA Binding Dyes such as SYBR Green I, TaqMan Probes and Molecular Beacons (including Scorpions).

The real time PCR thermal cycler has a fluorescence detection threshold, below which it cannot discriminate the difference between amplification generated signal and background noise. On the other hand, the fluorescence increases as the amplification progresses and the instrument performs data acquisition during the annealing step of each cycle. The number of amplicons will reach the detection baseline after a specific cycle, which depends on the initial concentration of the target DNA sequence. The cycle at which the instrument can discriminate the amplification generated fluorescence from the background noise is called the threshold cycle (Ct). The higher is the initial DNA concentration, the lower its Ct will be.

Other forms of nucleic acid detection can include next generation sequencing methods such as DNA SEQ or RNA SEQ using any known sequencing platform including, but not limited to: Roche 454, Solexa Genome Analyzer, AB SOLiD, Illumina GA/HiSeq, Ion PGM, Mi Seq, among others (Liu et al., 2012 Journal of Biomedicine and Biotechnology Volume 2012 ID 251364; Franca et al., 2002 Quarterly Reviews of Biophysics 35 pg 169-200; Mardis 2008 Genomics and Human Genetics vol 9 pg 387-402).

In other embodiments, nucleic acids may be detected with other high throughput hybridization technologies including microarrays, gene chips, LNA probes, nanoStrings, and fluorescence polarization detection among others.

In some embodiments, detection of markers can be achieved at an early stage of plant growth by harvesting a small tissue sample (e.g., branch, or leaf disk). This approach is preferable when working with large populations as it allows breeders to weed out undesirable progeny at an early stage and conserve growth space and resources for progeny which show more promise. In some embodiments the detection of markers is automated, such that the detection and storage of marker data is handled by a machine. Recent advances in robotics have also led to full service analysis tools capable of handling nucleic acid/protein marker extractions, detection, storage and analysis.

Quantitative Trait Loci

Breeding schemes of the present application can include crosses between donor and recipient plants. In some embodiments said donor plants contain a gene or genes of interest which may confer the plant with a desirable phenotype. The recipient line can be an elite line or cultivar having certain favorite traits such for commercial production. In one embodiment, the elite line may contain other genes that also impart said line with the desired phenotype. When crossed together, the donor and recipient plant may create a progeny plant with combined desirable loci which may provide quantitatively additive effect of a particular characteristic. In that case, QTL mapping can be involved to facilitate the breeding process.

A QTL (quantitative trait locus) mapping can be applied to determine the parts of the donor plant's genome conferring the desirable phenotype, and facilitate the breeding methods. Inheritance of quantitative traits or polygenic inheritance refers to the inheritance of a phenotypic characteristic that varies in degree and can be attributed to the interactions between two or more genes and their environment. Though not necessarily genes themselves, quantitative trait loci (QTLs) are stretches of DNA that are closely linked to the genes that underlie the trait in question. QTLs can be molecularly identified to help map regions of the genome that contain genes involved in specifying a quantitative trait. This can be an early step in identifying and sequencing these genes.

Typically, QTLs underlie continuous traits (those traits that vary continuously, e.g. yield, height, level of resistance to virus, etc.) as opposed to discrete traits (traits that have two or several character values, e.g. smooth vs. wrinkled peas used by Mendel in his experiments). Moreover, a single phenotypic trait is usually determined by many genes. Consequently, many QTLs are associated with a single trait.

A quantitative trait locus (QTL) is a region of DNA that is associated with a particular phenotypic trait—these QTLs are often found on different chromosomes. Knowing the number of QTLs that explains variation in the phenotypic trait tells about the genetic architecture of a trait. It may tell that a trait is controlled by many genes of small effect, or by a few genes of large effect.

Another use of QTLs is to identify candidate genes underlying a trait. Once a region of DNA is identified as contributing to a phenotype, it can be sequenced. The DNA sequence of any genes in this region can then be compared to a database of DNA for genes whose function is already known.

In a recent development, classical QTL analyses are combined with gene expression profiling i.e. by DNA microarrays. Such expression QTLs (e-QTLs) describes cis- and trans-controlling elements for the expression of often disease-associated genes. Observed epistatic effects have been found beneficial to identify the gene responsible by a cross-validation of genes within the interacting loci with metabolic pathway- and scientific literature databases.

QTL mapping is the statistical study of the alleles that occur in a locus and the phenotypes (physical forms or traits) that they produce (see, Meksem and Kahl, The handbook of plant genome mapping: genetic and physical mapping, 2005, Wiley-VCH, ISBN 3527311165, 9783527311163). Because most traits of interest are governed by more than one gene, defining and studying the entire locus of genes related to a trait gives hope of understanding what effect the genotype of an individual might have in the real world.

Statistical analysis is required to demonstrate that different genes interact with one another and to determine whether they produce a significant effect on the phenotype. QTLs identify a particular region of the genome as containing a gene that is associated with the trait being assayed or measured. They are shown as intervals across a chromosome, where the probability of association is plotted for each marker used in the mapping experiment.

To begin, a set of genetic markers must be developed for the species in question. A marker is an identifiable region of variable DNA. Biologists are interested in understanding the genetic basis of phenotypes (physical traits). The aim is to find a marker that is significantly more likely to co-occur with the trait than expected by chance, that is, a marker that has a statistical association with the trait. Ideally, they would be able to find the specific gene or genes in question, but this is a long and difficult undertaking. Instead, they can more readily find regions of DNA that are very close to the genes in question. When a QTL is found, it is often not the actual gene underlying the phenotypic trait, but rather a region of DNA that is closely linked with the gene.

For organisms whose genomes are known, one might now try to exclude genes in the identified region whose function is known with some certainty not to be connected with the trait in question. If the genome is not available, it may be an option to sequence the identified region and determine the putative functions of genes by their similarity to genes with known function, usually in other genomes. This can be done using BLAST, an online tool that allows users to enter a primary sequence and search for similar sequences within the BLAST database of genes from various organisms.

Another interest of statistical geneticists using QTL mapping is to determine the complexity of the genetic architecture underlying a phenotypic trait. For example, they may be interested in knowing whether a phenotype is shaped by many independent loci, or by a few loci, and do those loci interact. This can provide information on how the phenotype may be evolving.

Molecular markers are used for the visualization of differences in nucleic acid sequences. This visualization is possible due to DNA-DNA hybridization techniques (RFLP) and/or due to techniques using the polymerase chain reaction (e.g. STS, microsatellites, AFLP). All differences between two parental genotypes will segregate in a mapping population based on the cross of these parental genotypes. The segregation of the different markers may be compared and recombination frequencies can be calculated. The recombination frequencies of molecular markers on different chromosomes are generally 50%. Between molecular markers located on the same chromosome the recombination frequency depends on the distance between the markers. A low recombination frequency corresponds to a low distance between markers on a chromosome. Comparing all recombination frequencies will result in the most logical order of the molecular markers on the chromosomes. This most logical order can be depicted in a linkage map (Paterson, 1996, Genome Mapping in Plants. R. G. Landes, Austin.). A group of adjacent or contiguous markers on the linkage map that is associated to a reduced disease incidence and/or a reduced lesion growth rate pinpoints the position of a QTL.

The nucleic acid sequence of a QTL may be determined by methods known to the skilled person. For instance, a nucleic acid sequence comprising said QTL or a resistance-conferring part thereof may be isolated from a donor plant by fragmenting the genome of said plant and selecting those fragments harboring one or more markers indicative of said QTL. Subsequently, or alternatively, the marker sequences (or parts thereof) indicative of said QTL may be used as (PCR) amplification primers, in order to amplify a nucleic acid sequence comprising said QTL from a genomic nucleic acid sample or a genome fragment obtained from said plant. The amplified sequence may then be purified in order to obtain the isolated QTL. The nucleotide sequence of the QTL, and/or of any additional markers comprised therein, may then be obtained by standard sequencing methods.

One or more such QTLs associated with a desirable trait in a donor plant can be transferred to a recipient plant to make incorporate the desirable train into progeny plants by transferring and/or breeding methods.

In one embodiment, an advanced backcross QTL analysis (AB-QTL) is used to discover the nucleotide sequence or the QTLs responsible for the resistance of a plant. Such method was proposed by Tanksley and Nelson in 1996 (Tanksley and Nelson, 1996, Advanced backcross QTL analysis: a method for simultaneous discovery and transfer of valuable QTL from un-adapted germplasm into elite breeding lines. Theor Appl Genet 92:191-203) as a new breeding method that integrates the process of QTL discovery with variety development, by simultaneously identifying and transferring useful QTL alleles from un-adapted (e.g., land races, wild species) to elite germplasm, thus broadening the genetic diversity available for breeding. AB-QTL strategy was initially developed and tested in tomato, and has been adapted for use in other crops including rice, maize, wheat, pepper, barley, and bean. Once favorable QTL alleles are detected, only a few additional marker-assisted generations are required to generate near isogenic lines (NILs) or introgression lines (ILs) that can be field tested in order to confirm the QTL effect and subsequently used for variety development.

Isogenic lines in which favorable QTL alleles have been fixed can be generated by systematic backcrossing and introgressing of marker-defined donor segments in the recurrent parent background. These isogenic lines are referred as near isogenic lines (NILs), introgression lines (ILs), backcross inbred lines (BILs), backcross recombinant inbred lines (BCRIL), recombinant chromosome substitution lines (RCSLs), chromosome segment substitution lines (CSSLs), and stepped aligned inbred recombinant strains (STAIRSs). An introgression line in plant molecular biology is a line of a crop species that contains genetic material derived from a similar species. ILs represent NILs with relatively large average introgression length, while BILs and BCRILs are backcross populations generally containing multiple donor introgressions per line. As used herein, the term “introgression lines or ILs” refers to plant lines containing a single marker defined homozygous donor segment, and the term “pre-ILs” refers to lines which still contain multiple homozygous and/or heterozygous donor segments.

To enhance the rate of progress of introgression breeding, a genetic infrastructure of exotic libraries can be developed. Such an exotic library comprises of a set of introgression lines, each of which has a single, possibly homozygous, marker-defined chromosomal segment that originates from a donor exotic parent, in an otherwise homogenous elite genetic background, so that the entire donor genome would be represented in a set of introgression lines. A collection of such introgression lines is referred as libraries of introgression lines or IL libraries (ILLs). The lines of an ILL cover usually the complete genome of the donor, or the part of interest. Introgression lines allow the study of quantitative trait loci, but also the creation of new varieties by introducing exotic traits. High resolution mapping of QTL using ILLs enable breeders to assess whether the effect on the phenotype is due to a single QTL or to several tightly linked QTL affecting the same trait. In addition, sub-ILs can be developed to discover molecular markers which are more tightly linked to the QTL of interest, which can be used for marker-assisted breeding (MAB). Multiple introgression lines can be developed when the introgression of a single QTL is not sufficient to result in a substantial improvement in agriculturally important traits (Gur and Zamir, Unused natural variation can lift yield barriers in plant breeding, 2004, PLoS Biol.; 2(10):e245).

Tissue Culture

As is well known in the art, tissue culture of garden bean can be used for the in vitro regeneration of a garden bean plant. Tissue culture of various tissues of garden beans and regeneration of plants therefrom is well known and widely published. For example, reference may be had to McClean, P., Grafton, K. F., “Regeneration of dry bean (Phaseolus vulgaris) via organogenesis,” Plant Sci., 60, 117-122 (1989); Mergeai, G., Baudoin, J. P., “Development of an in vitro culture method for heart-shaped embryo in Phaseolus vulgaris,” B.I.C. Invit. Papers 33, 115-116 (1990); Vanderwesthuizen, A. J., Groenewald, E. G., “Root Formation and Attempts to Establish Morphogenesis in Callus Tissues of Beans (Phaseolus vulgaris L.),” S. Afr. J. Bot. 56, 271-273 (2 Apr. 1990); Benedicic, D., et al., “The regeneration of Phaseolus vulgaris L. plants from meristem culture,” Abst. 5th I.A.P.T.C. Cong. 1, 91 (# A3-33) (1990); Genga, A., Allavena, A., “Factors affecting morphogenesis from immature cotyledons of Phaseolus coccineus L.,” Abst. 5th I.A.P.T.C. Cong. 1, 101 (# A3-75) (1990); Vaquero, F., et al., “Plant regeneration and preliminary studies on transformation of Phaseolus coccineus,” Abst. 5th I.A.P.T.C. Cong. 1, 106 (# A3-93) (1990); Franklin, C. I., et al., “Plant Regeneration from Seedling Explants of Green Bean (Phaseolus-Vulgaris L.) via Organogenesis,” Plant Cell Tissue Org. Cult., 24, 199-206 (3 Mar. 1991); Malik, K. A., Saxena, P. K., “Regeneration in Phaseolus-vulgaris L.—Promotive Role of N6 Benzylaminopurine in Cultures from Juvenile Leaves,” Planta, 184(1), 148-150 (1991); Genga, A., Allavena, A., “Factors affecting morphogenesis from immature cotyledons of Phaseolus coccineus L.,” Plant Cell Tissue Org. Cult., 27, 189-196 (1991); Malik, K. A., Saxena, P. K., “Regeneration in Phaseolus vulgaris L.—High-Frequency Induction of Direct Shoot Formation in Intact Seedlings by N-6-Benzylaminopurine and Thidiazuron,” 186, 384-389 (3 Feb. 1992); Malik, K. A., Saxena, P. K., “Somatic Embryogenesis and Shoot Regeneration from Intact Seedlings of Phaseolus acutifolius A., P. aureus (L.) Wilczek, P. coccineus L., and P. wrightii L.,” Pl. Cell. Rep., 11, 163 168 (3 Apr. 1992); Chavez, J., et al., “Development of an in vitro culture method for heart shaped embryo in Phaseolus polyanthus,” B.I.C. Invit. Papers 35, 215-216 (1992); Munoz-Florez, L. C., et al., “Finding out an efficient technique for inducing callus from Phaseolus microspores,” B.I.C. Invit. Papers 35, 217-218 (1992); Vaquero, F., et al., “A Method for Long-Term Micropropagation of Phaseolus coccineus L.,” L. Pl. Cell. Rep., 12, 395-398 (7-8 May 1993); Lewis, M. E., Bliss, F. A., “Tumor Formation and beta-Glucuronidase Expression in Phaseolus vulgaris L. Inoculated with Agrobacterium Tumefaciens,” Journal of the American Society for Horticultural Science, 119, 361-366 (2 Mar. 1994); Song, J. Y., et al., “Effect of auxin on expression of the isopentenyl transferase gene (ipt) in transformed bean (Phaseolus vulgaris L.) single-cell clones induced by Agrobacterium tumefaciens C58,” J. Plant Physiol. 146, 148-154 (1-2 May 1995). It is clear from the literature that the state of the art is such that these methods of obtaining plants are routinely used and have a very high rate of success. Thus, another aspect of this invention is to provide cells which upon growth and differentiation produce garden bean plants having the physiological and morphological characteristics of garden bean cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494.

As used herein, the term “tissue culture” indicates a composition comprising isolated cells of the same or a different type or a collection of such cells organized into parts of a plant. Exemplary types of tissue cultures are protoplasts, calli, plant clumps, and plant cells that can generate tissue culture that are intact in plants or parts of plants, such as embryos, pollen, flowers, seeds, leaves, stems, roots, root tips, anthers, pistils, meristematic cells, axillary buds, ovaries, seed coat, endosperm, hypocotyls, cotyledons and the like. Means for preparing and maintaining plant tissue culture are well known in the art. By way of example, a tissue culture comprising organs has been used to produce regenerated plants. U.S. Pat. Nos. 5,959,185, 5,973,234, and 5,977,445 describe certain techniques, the disclosures of which are incorporated herein by reference.

EXAMPLES

The foregoing examples of the related art and limitations related therewith are intended to be illustrative and not exclusive. Other limitations of the related art will become apparent to those of skill in the art upon a reading of the specification.

Example 1—Development of Garden Bean Cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494

Development of Garden Bean Cultivar HMX4104

Breeding History:

Garden bean cultivar HMX4104 has superior characteristics and was developed from an initial cross that was made in Sun Prairie, Wis., in a greenhouse, in the fall. In the first year of development, the cross was made between two proprietary lines of Applicant under stake numbers 97513 (female) and 97503 (male), the F₁ generation was harvested in April in the greenhouse located in Sun Prairie, Wis., in plot 0192, and the F₂ selection was made in July near Coloma, Wis., in plot 018640. In the second year, the F₃ selection was made in November in the greenhouse located in Sun Prairie, Wis. in plot 09163; the F₄ selection was made in the greenhouse located in Sun Prairie, Wis. in plot 15231; and the F₅ selection was made near Coloma, Wis. in plot 104159. In the third year, the F₆ selection was made in February near Los Mochis, Mexico, in plot 20252 and the F₇ selection was made in July near Coloma, Wis., in plot 203969. In the fourth year, the F₈ generation was bulked in February near Los Mochis, Mexico, in plot 32609 and the F₉ generation was harvested as 100 single plants in August in Twin Falls, Id., in plots 304766 and 304767. In the fifth year, the F₁₀ generation was bulked by progeny row in February, near Los Mochis, Mexico, in plot 44101-148. The line was subsequently designated HMX4104.

Garden bean cultivar HMX4104 is similar to garden bean cultivar ‘Chisolm’. While similar to garden bean cultivar ‘Chisolm’, there are significant differences including garden bean cultivar HMX4104 is 3 days earlier than ‘Chisolm’ to edible pods.

Garden bean cultivar HMX4104 is a 52-day maturity bean with uniform medium dark green pods on an upright plant structure (habit). The pods are very straight and smooth and are borne in the upper one-half of the plant. The majority of the pods are in the 3, 4 and 5 sieve range. Garden bean cultivar HMX4104 is a determinate plant and is resistant to Bean Common Mosaic Virus (BCMV I-gene) and Beet Curly Top Virus (BCTV). HMX4104 has Intermediate Resistant to Pseudomonas syringae pv syringae and Pseudomonas syringae pv phaseolicola.

The garden bean cultivar HMX4104 has shown uniformity and stability for the traits, within the limits of environmental influence for the traits as described in the following Variety Descriptive Information. No variant traits have been observed or are expected for agronomical important traits in garden bean cultivar HMX4104.

Garden bean cultivar HMX4104, has the following morphologic and other characteristics, (based primarily on data collected in Coloma and Sun Prairie, Wis., all experiments done under the direct supervision of the applicant).

TABLE 1 Variety Description Information for HMX4104 Market Maturity: Days to edible pods 52 Number of days earlier than “Chisolm” 4 Plant: Habit Determinate Pod position Medium-High Bush form High Bush Leaves: Surface: Semi-glossy Size: Medium Color: Medium dark-green Anthocyanin Pigment: Flower Absent Stem Absent Pods Absent Seeds Absent Leaves Absent Petioles Absent Peduncles Absent Nodes Absent Flower color: Color of standard White Color of wings White Color of keel White Pods (edible maturity): Exterior color Medium dark-green Cross section pod shape Round Creaseback Present Pubescence Sparse Constriction None Spur length 12 mm Fiber Sparse Number of seeds/pods 6 Suture string Absent Seed development Medium Machine harvest Adapted Distribution of sieve size at optimum maturity 7.34 mm to 8.34 mm - Sieve 3 14 8.34 mm to 9.53 mm - Sieve 4 21 9.53 mm to 10.72 mm - Sieve 5 65 Seed Color: Seed coat luster Semi-shiny Seed coat Monchrome Primary color Green Seed coat pattern Solid Hilar ring Absent Seed Shape and Size Hilum view Oval Cross section Oval Side view Oval Seed size (g/100 seeds) 32 Disease Resistance Bean Common Mosaic Virus (BCMV I gene) Beet Curly Top Virus (BCTV) Pseudomonas syringae pv syringae Pseudomonas syringae pv phaseolicola Development of Garden Bean Cultivar HMX0164423 Breeding History:

Garden bean cultivar HMX0164423 has superior characteristics and was developed from an initial cross that was made in Sun Prairie, Wis., in a greenhouse, in the fall. In the first year of development, the cross was made between two proprietary lines of Applicant under stake numbers 97494 (female) and 97483 (male), the F₁ generation was harvested in April in the greenhouse located in Sun Prairie, Wis., in plot 0151, and the F₂ selection was made in July near Coloma, Wis., in plot 018305. In the second year, the F₃ selection was made in July near Coloma, Wis., in plot 105422. In the third year, the F₄ selection was made in February near Los Mochis, Mexico, in plot 20821 and the F₅ selection was made in July near Coloma, Wis., in plot 204317. In the fourth year, the F₆ selection was made in February near Los Mochis, Mexico, in plot 30195 and the F₇ selection was made in July near Coloma, Wis., in plot 305452. In the fifth year, the F₈ generation was bulked in February near Los Mochis, Mexico, in plot 42883 and the F₉ generation was harvested as 150 single plants in August in Twin Falls, Id., in plots 508295, 508296, 508297, and 508298. In the sixth year, the F₁₀ generation was bulked by progeny row in February, near Los Mochis, Mexico, in plot 63501-548. The line was subsequently designated HMX0164423.

Garden bean cultivar HMX0164423 is similar to garden bean cultivar ‘Bowie’. While similar to garden bean cultivar ‘Bowie’, there are significant differences including garden bean cultivar HMX0164423 has pods 5 millimeters longer than ‘Bowie’ and is 2 days earlier in edible maturity.

Garden bean cultivar HMX0164423 is a 55-day maturity bean with uniform medium dark green pods on an upright plant structure (habit). The pods are very straight and smooth and are borne in the upper one-half of the plant. The majority of the pods are in the 3, 4 and 5 sieve range. The leaves are medium in size with a medium-dark green color. Garden bean cultivar HMX0164423 is a determinate plant and is resistant to Bean Common Mosaic Virus (BCMV I-gene), Beet Curly Top Virus (BCTV) and Colletotrichum lindemuthianum (races 7 and 73). HMX0164423 has Intermediate Resistant to Pseudomonas syringae pv syringae.

The garden bean cultivar HMX0164423 has shown uniformity and stability for the traits, within the limits of environmental influence for the traits as described in the following Variety Descriptive Information. No variant traits have been observed or are expected for agronomical important traits in garden bean cultivar HMX0164423.

Garden bean cultivar HMX0164423, has the following morphologic and other characteristics, (based primarily on data collected in Coloma and Sun Prairie, Wis., all experiments done under the direct supervision of the applicant).

TABLE 2 Variety Description Information for HMX0164423 Market Maturity: Days to edible pods 55 Number of days earlier than “Bowie” 2 Plant: Habit Determinate Pod position Medium-High Bush form High Bush Leaves: Surface: Semi-Glossy Size: Medium Color: Medium dark-green Anthocyanin Pigment: Flower Absent Stem Absent Pods Absent Seeds Absent Leaves Absent Petioles Absent Peduncles Absent Nodes Absent Flower color: Color of standard White Color of wings White Color of keel White Pods (edible maturity): Exterior color Dark green Cross section pod shape Round Creaseback Present Pubescence Sparse Constriction None Spur length 10 mm Fiber Sparse Number of seeds/pods 6 Suture string Absent Seed development Slow Machine harvest Adapted Distribution of sieve size at optimum maturity 7.34 mm to 8.34 mm - Sieve 3 35 8.34 mm to 9.53 mm - Sieve 4 51 9.53 mm to 10.72 mm - Sieve 5 14 Seed Color: Seed coat luster Shiny Seed coat Monchrome Primary color White Seed coat pattern Solid Hilar ring Absent Seed Shape and Size Hilum view Oval Cross section Oval Side view Oblong Seed size (g/100 seeds) 30 Disease Resistance Bean Common Mosaic Virus (BCMV I gene) Beet Curly Top Virus (BCTV) Colletotrichum Lindemuthianum (races 7 and 73) Pseudomonas syringae pv syringae Development of Garden Bean Cultivar HMX0164444 Breeding History:

Garden bean cultivar HMX0164444 has superior characteristics and was developed from an initial cross that was made in Sun Prairie, Wis., in a greenhouse, in the fall. In the first year of development, the cross was made between two proprietary lines of Applicant under stake numbers 97517 (female) and 97505 (male), the F₁ generation was harvested in April in the greenhouse located in Sun Prairie, Wis., in plot 0221, and the F₂ selection was made in July near Coloma, Wis., in plot 018884. In the second year, the F₃ selection was made in July near Coloma, Wis., in plot 105945. In the third year, the F₄ selection was made in February near Los Mochis, Mexico, in plot 20963 and the F₅ selection was made in July near Coloma, Wis., in plot 204388. In the fourth year, the F₆ selection was made in February near Los Mochis, Mexico, in plot 30238 and the F₇ selection was made in July near Coloma, Wis., in plot 305497. In the fifth year, the F₈ generation was bulked in February near Los Mochis, Mexico, in plot 42911. In the sixth year, the F₉ generation was bulked in February near Los Mochis, Mexico, in plot 53124 and the F₁₀ generation was harvested as 150 single plants in August in Twin Falls, Id., in plots 508315, 508316, 508317, and 508318. In the sixth year, the F₁₁ generation was bulked by progeny row in February, near Los Mochis, Mexico, in plot 63601-648. The line was subsequently designated HMX0164444.

Garden bean cultivar HMX0164444 is similar to garden bean cultivar ‘Wyatt’. While similar to garden bean cultivar ‘Wyatt’, there are significant differences including garden bean cultivar HMX0164444 has medium dark green pods while ‘Wyatt’ has dark green pods. The pods of HMX0164444 are 10 millimeters shorter than ‘Wyatt’ pods.

Garden bean cultivar HMX0164444 is a 56-day maturity bean with uniform medium dark green pods on an upright plant structure (habit). The pods are very straight and smooth and are borne in the upper one-half of the plant. The majority of the pods are in the 3, 4 and 5 sieve range. The leaves are medium in size with a medium-dark green color. Garden bean cultivar HMX0164444 is a determinate plant and is resistant to Bean Common Mosaic Virus (BCMV I-gene) and Beet Curly Top Virus (BCTV). HMX0164444 has Intermediate Resistant to Pseudomonas syringae pv syringae and Colletotrichum lindemuthianum (races 7 and 73).

The garden bean cultivar HMX0164444 has shown uniformity and stability for the traits, within the limits of environmental influence for the traits as described in the following Variety Descriptive Information. No variant traits have been observed or are expected for agronomical important traits in garden bean cultivar HMX0164444.

Garden bean cultivar HMX0164444, has the following morphologic and other characteristics, (based primarily on data collected in Coloma and Sun Prairie, Wis., all experiments done under the direct supervision of the applicant).

TABLE 3 Variety Description Information for HMX0164444 Market Maturity: Days to edible pods 56 Number of days later than “Wyatt” 1 Plant: Habit Determinate Pod position Medium-high Bush form High Bush Leaves: Surface: Semi-glossy Size: Medium Color: Medium dark-green Anthocyanin Pigment: Flower Absent Stem Absent Pods Absent Seeds Absent Leaves Absent Petioles Absent Peduncles Absent Nodes Absent Flower color: Color of standard White Color of wings White Color of keel White Pods (edible maturity): Exterior color Medium dark-green Cross section pod shape Round Creaseback Present Pubescence Sparse Constriction None Spur length 11 mm Fiber Sparse Number of seeds/pods 6 Suture string Absent Seed development Slow Machine harvest Adapted Distribution of sieve size at optimum maturity 7.34 mm to 8.34 mm - Sieve 3 40 8.34 mm to 9.53 mm - Sieve 4 49 9.53 mm to 10.72 mm - Sieve 5 11 Seed Color: Seed coat luster Shiny Seed coat Monochrome Primary color White Seed coat pattern Solid Hilar ring Absent Seed Shape and Size Hilum view Oval Cross section Oval Side view Oval Seed size (g/100 seeds) 26 Disease Resistance Bean Common Mosaic Virus (BCMV I gene) Beet Curly Top Virus (BCTV) Colletotrichum lindemuthianum (races 7 and 73) Pseudomonas syringae pv syringae Development of Garden Bean Cultivar HMX0164476 Breeding History:

Garden bean cultivar HMX0164476 has superior characteristics and was developed from an initial cross that was made in Sun Prairie, Wis., in a greenhouse, in the fall. In the first year of development, the cross was made between two proprietary lines of Applicant under stake numbers 09561 (female) and 09577 (male), the F₁ generation was harvested in April in the greenhouse located in Sun Prairie, Wis., in plot 1016, and the F₂ selection was made in July near Coloma, Wis., in plot 109737. In the second year, the F₃ selection was made in February near Los Mochis, Mexico, in plot 21231 and the F₄ selection was made in July near Coloma, Wis., in plot 204640. In the third year, the F₅ selection was made in February near Los Mochis, Mexico, in plot 30223 and the F₆ selection was made in July near Coloma, Wis., in plot 305567. In the fourth year, the F₇ generation was bulked in February near Los Mochis, Mexico, in plot 42951. In the fifth year, the F₈ generation was bulked in February near Los Mochis, Mexico, in plot 53110 and the F₉ generation was harvested as 150 single plants in August in Twin Falls, Id., in plots 508183, 508184, 508185, and 508186. In the sixth year, the F₁₀ generation was bulked by progeny row in February, near Los Mochis, Mexico, in plot 63301-348. The line was subsequently designated HMX0164476.

Garden bean cultivar HMX0194476 is similar to garden bean cultivar ‘Chisolm’. While similar to garden bean cultivar ‘Chisolm’, there are significant differences including garden bean cultivar HMX0164476 has medium green pods while ‘Chisolm’ has dark green pods.

Garden bean cultivar HMX0164476 is a 56-day maturity bean with uniform medium green pods on an upright plant structure (habit). The pods are very straight and smooth and are borne in the upper one-half of the plant. The majority of the pods are in the 3, 4 and 5 sieve range. The leaves are medium in size with a medium-dark green color. Garden bean cultivar HMX0164476 is a determinate plant and is resistant to Bean Common Mosaic Virus (BCMV I-gene), Beet Curly Top Virus (BCTV), and Pseudomonas syringae pv syringae.

The garden bean cultivar HMX0164476 has shown uniformity and stability for the traits, within the limits of environmental influence for the traits as described in the following Variety Descriptive Information. No variant traits have been observed or are expected for agronomical important traits in garden bean cultivar HMX0164476.

Garden bean cultivar HMX0164476, has the following morphologic and other characteristics, (based primarily on data collected in Coloma and Sun Prairie, Wis., all experiments done under the direct supervision of the applicant).

TABLE 4 Variety Description Information for HMX0164476 Market Maturity: Days to edible pods 56 Number of days later than “Chisolm” 0 Plant: Habit Determinate Pod position Medium-High Bush form High Bush Leaves: Surface: Semi-glossy Size: Medium Color: Medium dark-green Anthocyanin Pigment: Flower Absent Stem Absent Pods Absent Seeds Absent Leaves Absent Petioles Absent Peduncles Absent Nodes Absent Flower color: Color of standard White Color of wings White Color of keel White Pods (edible maturity): Exterior color Medium green Cross section pod shape Round Creaseback Present Pubescence Sparse Constriction None Spur length 12 mm Fiber Sparse Number of seeds/pods 7 Suture string Absent Seed development Slow Machine harvest Adapted Distribution of sieve size at optimum maturity 7.34 mm to 8.34 mm - Sieve 3 20 8.34 mm to 9.53 mm - Sieve 4 28 9.53 mm to 10.72 mm - Sieve 5 52 Seed Color: Seed coat luster Shiny Seed coat Monochrome Primary color White Seed coat pattern Solid Hilar ring Absent Seed Shape and Size Hilum view Oval Cross section Oval Side view Oval Seed size (g/100 seeds) 36 Disease Resistance Bean Common Mosaic Virus (BCMV I gene) Beet Curly Top Virus (BCTV) Pseudomonas syringae pv syringae Development of Garden Bean Cultivar HMX0164494 Breeding History:

Garden bean cultivar HMX0164494 has superior characteristics and was developed from an initial cross that was made in Sun Prairie, Wis., in a greenhouse, in the fall. In the first year of development, the cross was made between two proprietary lines of Applicant under stake numbers 09567 (female) and 09576 (male), the F₁ generation was harvested in April in the greenhouse located in Sun Prairie, Wis., in plot 1062, and the F₂ selection was made in July near Coloma, Wis., in plot 110158. In the second year, the F₃ selection was made in February near Los Mochis, Mexico, in plot 21607 and the F₄ selection was made in July near Coloma, Wis., in plot 204799. In the third year, the F₅ selection was made in February near Los Mochis, Mexico, in plot 30410 and the F₆ selection was made in July near Coloma, Wis., in plot 305638. In the fourth year, the F₇ generation was bulked in February near Los Mochis, Mexico, in plot 42973. In the fifth year, the F₈ generation was bulked in February near Los Mochis, Mexico, in plot 53107 and the F₉ generation was harvested as 150 single plants in August in Twin Falls, Id., in plots 508191, 508192, 508193, and 508194. In the sixth year, the F₁₀ generation was bulked by progeny row in February, near Los Mochis, Mexico, in plot 63401-448. The line was subsequently designated HMX0164494.

Garden bean cultivar HMX0164494 is similar to garden bean cultivar ‘Caprice’. While similar to garden bean cultivar ‘Caprice’, there are significant differences including garden bean cultivar HMX0164494 has 45 percent 5 sieve pods while ‘Caprice’ has 22 percent.

Garden bean cultivar HMX0164494 is a 56-day maturity bean with uniform medium dark green pods on an upright plant structure (habit). The pods are very straight and smooth and are borne in the upper one-half of the plant. The majority of the pods are in the 3, 4 and 5 sieve range. The leaves are medium in size with a medium-dark green color. Garden bean cultivar HMX0164494 is a determinate plant and is resistant to Bean Common Mosaic Virus (BCMV I-gene), Colletotrichum lindemuthianum (races 7 and 73) and Pseudomonas syringae pv syringae.

The garden bean cultivar HMX0164494 has shown uniformity and stability for the traits, within the limits of environmental influence for the traits as described in the following Variety Descriptive Information. No variant traits have been observed or are expected for agronomical important traits in garden bean cultivar HMX0164494.

Garden bean cultivar HMX0164494, has the following morphologic and other characteristics, (based primarily on data collected in Coloma and Sun Prairie, Wis., all experiments done under the direct supervision of the applicant).

TABLE 5 Variety Description Information for HMX0164494 Market Maturity: Days to edible pods 56 Number of days later than “Caprice” 0 Plant: Habit Determinate Pod position Medium-high Bush form High Bush Leaves: Surface: Semi-glossy Size: Medium Color: Medium dark-green Anthocyanin Pigment: Flower Absent Stem Absent Pods Absent Seeds Absent Leaves Absent Petioles Absent Peduncles Absent Nodes Absent Flower color: Color of standard White Color of wings White Color of keel White Pods (edible maturity): Exterior color Medium dark-green Cross section pod shape Round Creaseback Present Pubescence Sparse Constriction None Spur length 12 mm Fiber Sparse Number of seeds/pods 6 Suture string Absent Seed development Slow Machine harvest Adapted Distribution of sieve size at optimum maturity 7.34 mm to 8.34 mm - Sieve 3 20 8.34 mm to 9.53 mm - Sieve 4 35 9.53 mm to 10.72 mm - Sieve 5 45 Seed Color: Seed coat luster Dull Seed coat Monochrome Primary color White Seed coat pattern Solid Hilar ring Absent Seed Shape and Size Hilum view Oval Cross section Oval Side view Oval Seed size (g/100 seeds) 30 Disease Resistance Bean Common Mosaic Virus (BCMV I gene) Colletotrichum lindemuthianum (races 7 and 73) Pseudomonas syringae pv syringae

Example 2—Field Trials Characteristics of Garden Bean Cultivar HMX4104, HMX0164423, HMX0164444, HMX0164476 and/or HMX0164494

Field Trials Characteristics of Garden Bean Cultivar HMX4104

In Table 6, the traits and characteristics of garden bean cultivar HMX4104 are compared to the ‘Chisolm’ variety of garden beans. The data was collected from two field locations in the United States. The field tests are experimental trials and have been made under supervision of the applicant.

The first column shows the variety name.

The second column shows the location of testing. “Heath” indicates Coloma, Wis. and “SunPrairie” indicates Sun Prairie, Wis. The number “1”, “2”, or “3” indicates the first, second, or third planting at the location.

The third column shows the plant height in inches.

The fourth column shows the plant width in inches.

The fifth column indicates the plant habit (structure) with 1=prone (or sprawling) and 9=upright (or erect).

The sixth column indicates the pod length in millimeters.

The seventh column shows the relative pod color with 1=light and 9=dark.

The eighth column shows the relative maturity (the number of days to edible pods).

The ninth column shows the percentage of pods <8.34 mm in diameter

The tenth column shows the percentage of pods between 8.34 mm to 9.53 mm

The eleventh column shows the percentage of pods >9.53 mm

TABLE 6 Characteristic Comparisons for Field Trials Plant Plant Plant Pod Pod Sieve Sieve Sieve Variety LOCATION Height Width Habit Length Color Maturity 1-3% 4% 5% HMX4104 Heath1 13 16 6 155 7 60 15 18 68 Heath2 16 17 6 145 7 60 15 27 59 SunPrairie1 16 20 6 170 8 58 8 16 77 SunPrairie2 18 21 5 150 6 55 15 22 63 SunPrairie3 17 21 7 145 7 53 17 24 59 16.0 19.0 6.0 153.0 7.0 57.2 14 21 65 Chisolm Heath1 14 17 6 160 7 62 14 19 67 Heath2 18 19 6 145 7 60 15 23 62 SunPrairie1 17 21 6 155 7 67 18 35 47 SunPrairie2 18 21 5 160 8 57 10 17 73 SunPrairie3 20 20 6 150 7 55 24 24 52 17.4 19.6 5.8 154.0 7.2 60.2 16 24 60 Field Trials Characteristics of Garden Bean Cultivar HMX0164423

In Table 7, the traits and characteristics of garden bean cultivar HMX0164423 are compared to the ‘Bowie’ variety of garden beans. The data was collected from two field locations in the United States. The field tests are experimental trials and have been made under supervision of the applicant.

The first column shows the variety name.

The second column shows the location of testing. “Heath” indicates Coloma, Wis. and “SunPrairie” indicates Sun Prairie, Wis. The number “1”, “2”, or “3” indicates the first, second, or third planting at the location.

The third column shows the plant height in inches.

The fourth column shows the plant width in inches.

The fifth column indicates the plant habit (structure) with 1=prone (or sprawling) and 9=upright (or erect).

The sixth column indicates the pod length in millimeters.

The seventh column shows the relative pod color with 1=light and 9=dark.

The eighth column shows the relative maturity (the number of days to edible pods).

The ninth column shows the percentage of pods <8.34 mm in diameter

The tenth column shows the percentage of pods between 8.34 mm to 9.53 mm

The eleventh column shows the percentage of pods >9.53 mm

TABLE 7 Characteristic Comparisons for Field Trials Plant Plant Plant Pod Pod Sieve Sieve Sieve Variety LOCATION Height Width Habit Length Color Maturity 1-3% 4% 5% HMX0164423 Heath1 14 18 5 130 7 60 38 44 18 Heath2 17 18 6 140 8 60 36 54 10 SunPrairie1 19 21 6 145 8 64 30 60 9 SunPrairie2 17 19 6 135 8 58 35 55 10 SunPrairie3 21 22 6 150 7 55 35 40 25 17.6 19.6 5.8 140.0 7.6 59.4 35 51 14 Bowie Heath1 13 16 5 130 7 64 39 54 7 Heath2 18 20 6 135 8 61 32 56 12 SunPrairie1 17 20 6 145 8 67 32 58 10 SunPrairie2 17 19 6 130 7 60 40 48 12 SunPrairie3 22 24 7 135 7 56 39 49 12 17.4 19.8 6.0 135.0 7.4 61.6 36 53 11 Field Trials Characteristics of Garden Bean Cultivar HMX0164444

In Table 8, the traits and characteristics of garden bean cultivar HMX0164444 are compared to the ‘Wyatt’ variety of garden beans. The data was collected from two field locations in the United States. The field tests are experimental trials and have been made under supervision of the applicant.

The first column shows the variety name.

The second column shows the location of testing. “Heath” indicates Coloma, Wis. and “SunPrairie” indicates Sun Prairie, Wis. The number “1”, “2”, or “3” indicates the first, second, or third planting at the location.

The third column shows the plant height in inches.

The fourth column shows the plant width in inches.

The fifth column indicates the plant habit (structure) with 1=prone (or sprawling) and 9=upright (or erect).

The sixth column indicates the pod length in millimeters.

The seventh column shows the relative pod color with 1=light and 9=dark.

The eighth column shows the relative maturity (the number of days to edible pods).

The ninth column shows the percentage of pods <8.34 mm in diameter

The tenth column shows the percentage of pods between 8.34 mm to 9.53 mm

The eleventh column shows the percentage of pods >9.53 mm

TABLE 8 Characteristic Comparisons for Field Trials Plant Plant Plant Pod Pod Sieve Sieve Sieve Variety LOCATION Height Width Habit Length Color Maturity 1-3% 4% 5% HMX0164444 Heath1 15 17 5 115 6 64 40 51 9 Heath2 18 18 5 135 5 63 38 51 11 SunPrairie1 18 21 5 140 6 66 38 48 14 SunPrairie2 20 21 5 140 6 58 38 57 5 SunPrairie3 20 23 5 140 6 56 47 36 17 18.2 20.0 5.0 134.0 5.8 61.4 40 49 11 Wyatt Heath1 14 15 5 145 9 63 47 44 9 Heath2 18 18 7 140 9 62 27 73 0 SunPrairie1 17 20 5 140 8 66 18 45 37 SunPrairie2 19 19 5 150 8 58 26 61 13 SunPrairie3 18 20 5 150 8 55 27 38 36 17.2 18.4 5.4 145.0 8.4 60.8 29 52 19 Field Trials Characteristics of Garden Bean Cultivar HMX0164476

In Table 9, the traits and characteristics of garden bean cultivar HMX0164476 are compared to the ‘Chisolm’ variety of garden beans. The data was collected from two field locations in the United States. The field tests are experimental trials and have been made under supervision of the applicant.

The first column shows the variety name.

The second column shows the location of testing. “Heath” indicates Coloma, Wis. and “SunPrairie” indicates Sun Prairie, Wis. The number “1”, “2”, or “3” indicates the first, second, or third planting at the location.

The third column shows the plant height in inches.

The fourth column shows the plant width in inches.

The fifth column indicates the plant habit (structure) with 1=prone (or sprawling) and 9=upright (or erect).

The sixth column indicates the pod length in millimeters.

The seventh column shows the relative pod color with 1=light and 9=dark.

The eighth column shows the relative maturity (the number of days to edible pods).

The ninth column shows the percentage of pods <8.34 mm in diameter

The tenth column shows the percentage of pods between 8.34 mm to 9.53 mm

The eleventh column shows the percentage of pods >9.53 mm

TABLE 9 Characteristic Comparisons for Field Trials Plant Plant Plant Pod Pod Sieve Sieve Sieve Variety LOCATION Height Width Habit Length Color Maturity 1-3% 4% 5% HMX0164476 Heath1 13 15 6 130 8 62 25 36 39 Heath2 17 21 5 150 7 61 29 31 40 SunPrairie1 18 20 5 160 6 64 19 36 45 SunPrairie2 19 25 4 165 5 58 12 17 71 SunPrairie3 19 18 5 155 6 55 16 22 62 17.2 19.8 5.0 152.0 6.4 60.0 20 28 51 Chisolm Heath1 14 17 6 160 7 62 14 19 67 Heath2 18 19 6 145 7 60 15 23 62 SunPrairie1 17 21 6 155 7 67 18 35 47 SunPrairie2 18 21 5 160 8 57 10 17 73 SunPrairie3 20 20 6 150 7 55 24 24 52 17.4 19.6 5.8 154.0 7.2 60.2 16 24 60 Field Trials Characteristics of Garden Bean Cultivar HMX0164494

In Table 10, the traits and characteristics of garden bean cultivar HMX0164494 are compared to the ‘Caprice’ variety of garden beans. The data was collected from two field locations in the United States. The field tests are experimental trials and have been made under supervision of the applicant.

The first column shows the variety name.

The second column shows the location of testing. “Heath” indicates Coloma, Wis. and “SunPrairie” indicates Sun Prairie, Wis. The number “1”, “2”, or “3” indicates the first, second, or third planting at the location.

The third column shows the plant height in inches.

The fourth column shows the plant width in inches.

The fifth column indicates the plant habit (structure) with 1=prone (or sprawling) and 9=upright (or erect).

The sixth column indicates the pod length in millimeters.

The seventh column shows the relative pod color with 1=light and 9=dark.

The eighth column shows the relative maturity (the number of days to edible pods).

The ninth column shows the percentage of pods <8.34 mm in diameter

The tenth column shows the percentage of pods between 8.34 mm to 9.53 mm

The eleventh column shows the percentage of pods >9.53 mm

TABLE 10 Characteristic Comparisons for Field Trials Plant Plant Plant Pod Pod Sieve Sieve Sieve Variety LOCATION Height Width Habit Length Color Maturity 1-3% 4% 5% 4494 Heath1 15 17 6 140 6 61 18 40 42 Heath2 20 21 5 135 6 60 19 39 42 SunPrairie1 17 21 6 140 6 65 16 30 54 SunPrairie2 17 22 4 145 6 57 20 29 52 SunPrairie3 20 19 5 145 6 56 29 35 37 17.8 20.0 5.2 141.0 6.0 59.8 20 35 45 Caprice Heath1 14 15 6 130 7 60 35 50 15 Heath2 16 19 6 140 6 60 31 59 9 SunPrairie1 18 22 6 150 7 67 27 52 21 SunPrairie2 17 21 6 140 7 58 20 48 32 SunPrairie3 19 21 5 140 6 54 23 45 32 16.8 19.6 5.8 140.0 6.6 59.8 27 51 22 Deposit Information

A deposit of the garden bean seeds of this invention is maintained by HM.CLAUSE, INC., 260 Cousteau Place, Suite 100, Davis, Calif. 95618. In addition, a sample of the garden bean seed of this invention has been deposited with the National Collections of Industrial, Food and Marine Bacteria (NCIMB), 23 St Machar Drive, Aberdeen, Scotland, AB24 3RY, United Kingdom.

To satisfy the enablement requirements of 35 U.S.C. 112, and to certify that the deposit of the isolated strain of the present invention meets the criteria set forth in 37 C.F.R. 1.801-1.809, Applicants hereby make the following statements regarding the deposited garden bean cultivar HMX0164494 (deposited as NCIMB Accession No. 43481):

1. During the pendency of this application, access to the invention will be afforded to the Commissioner upon request;

2. All restrictions on availability to the public will be irrevocably removed upon granting of the patent under conditions specified in 37 CFR 1.808;

3. The deposit will be maintained in a public repository for a period of 30 years or 5 years after the last request or for the effective life of the patent, whichever is longer;

4. A test of the viability of the biological material at the time of deposit will be conducted by the public depository under 37 C.F.R. 1.807; and

5. The deposit will be replaced if it should ever become unavailable.

Access to this deposit will be available during the pendency of this application to persons determined by the Commissioner of Patents and Trademarks to be entitled thereto under 37 C.F.R. § 1.14 and 35 U.S.C. § 122. Upon allowance of any claims in this application, all restrictions on the availability to the public of the variety will be irrevocably removed by affording access to a deposit of at least 2,500 seeds of the same variety with the NCIMB.

INCORPORATION BY REFERENCE

All references, articles, publications, patents, patent publications, and patent applications cited herein are incorporated by reference in their entireties for all purposes.

However, mention of any reference, article, publication, patent, patent publication, and patent application cited herein is not, and should not be taken as an acknowledgment or any form of suggestion that they constitute valid prior art or form part of the common general knowledge in any country in the world. 

What is claimed is:
 1. A seed of garden bean cultivar designated HMX0164494, wherein a representative sample of seed of said garden bean having been deposited under NCIMB No.
 43481. 2. A garden bean plant, or a plant part thereof or a plant cell thereof, produced by growing the seed of claim
 1. 3. The garden bean part of claim 2, wherein the garden bean plant part is selected from the group consisting of a leaf, a flower, a pod, an ovule, a cell and pollen.
 4. A garden bean plant, or a plant part or a plant cell thereof, wherein the garden bean plant or a garden bean plant regenerated from the plant part or plant cell has all of the characteristics of garden bean HMX0164494 listed in Table 5 when grown in the same environmental condition, wherein a representative sample of seed of HMX0164494 has been deposited under NCIMB No.
 43481. 5. A garden bean plant, or a part thereof, having all of the physiological and morphological characteristics of garden bean HMX0164494, wherein a representative sample of seed of said bean having been deposited under NCIMB No.
 43181. 6. A tissue culture of regenerable cells produced from the plant or plant part of claim 2, wherein cells of the tissue culture are produced from a plant part, wherein a plant regenerated from the tissue culture has all of the characteristics of garden bean HMX0164494 listed in Table 5 when grown in the same environmental condition, and wherein a representative sample of seed of said bean having been deposited under NCIMB No.
 43481. 7. A garden bean plant regenerated from the tissue culture of claim 6, said plant having all of the morphological and physiological characteristics of garden bean HMX0164494, wherein a representative sample of seed of said bean having been deposited under NCIMB No.
 43481. 8. A garden bean pod produced from the plant of claim
 2. 9. A method for producing a garden bean pod, the method comprising: (a) growing the bean plant of claim 2 to produce a garden bean pod, and (b) harvesting said bean pod.
 10. A garden bean pod produced by the method of claim
 9. 11. A method for producing a garden bean seed, the method comprising: crossing a first parent garden bean plant with a second parent garden bean plant and harvesting the resultant garden bean seed, wherein said first parent garden bean plant and/or second parent garden bean plant is the garden bean plant of claim
 2. 12. The garden bean seed produced by the method of claim
 11. 13. A method for producing a garden bean seed, the method comprising: self-pollinating the garden bean plant of claim 2 and harvesting the resultant garden bean seed.
 14. A garden bean seed produced by the method of claim
 13. 15. A method of producing a garden bean plant derived from the garden bean HMX0164494, the method comprising the steps of: (a) crossing the plant of claim 2 with a second garden bean plant to produce a progeny plant; (b) crossing the progeny plant of step (a) with itself or a second garden bean plant to produce a seed; (c) growing a progeny plant of a subsequent generation from the seed produced in step (b); (d) crossing the progeny plant of a subsequent generation of step (c) with itself or a second garden bean plant to produce a garden bean plant derived from the garden bean HMX0164494.
 16. The method of claim 15 further comprising the step of: (e) repeating step (b) and/or (c) for at least 1 more generation to produce a garden bean plant derived from the garden bean HMX0164494.
 17. The garden bean plant of claim 2, comprising: at least one single locus conversion, wherein the plant comprises the at least one single locus conversion, and otherwise all of the characteristics of HMX0164494 listed in Table 5 when grown under the same environmental conditions.
 18. The garden bean plant of claim 17, wherein the at least one single locus conversion confers said plant with a trait selected from the group consisting of male sterility, male fertility, herbicide resistance, insect resistance, disease resistance, water stress tolerance, heat tolerance, improved shelf life, delayed shelf life and improved nutritional quality.
 19. The garden bean plant of claim 17, wherein the at least one single locus conversion is an artificially mutated gene.
 20. The garden bean plant of claim 17, wherein the at least one single locus conversion is a gene that has been modified through the use of new breeding techniques.
 21. A method of introducing a desired trait into garden bean HMX0164494, the method comprising the steps of: (a) crossing a garden bean HMX0164494 plant grown from garden bean HMX0164494 seed, wherein a representative sample of seed has been deposited under NCIMB No. 43481 with another bean plant that comprises a desired trait to produce F1 progeny plants, wherein the desired trait is selected from the group consisting of insect resistance, disease resistance, water stress tolerance, heat tolerance, improved shelf life delayed shelf life, and improved nutritional quality; (b) selecting one or more progeny plants that have the desired trait to produce selected progeny plants; (c) crossing the selected progeny plants with the garden bean HMX0164494 plant to produce backcross progeny plants; (d) selecting for backcross progeny plants that have the desired trait and the physiological and morphological characteristics of garden bean HMX0164494 listed in Table 5 when grown in the same environmental condition to produce selected backcross progeny plants; and (e) repeating steps (c) and (d) three or more times in succession to produce selected fourth or higher backcross progeny plants that comprise the desired trait and the physiological and morphological characteristics of garden bean HMX0164494 listed in Table 5 when grown in the same environmental condition. 